ADVANCE Blog Notes: Interesting article by Mary Ann Mason at Slate.Com "In the Ivory Tower, Men Only"

There is a really interesting article at Slate.Com from Mary Ann Mason, the author of “Do Babies Matter” which I have written about here before.  The post is titled “In the Ivory Tower, Men Only“.  The post tells some of the background behind the book and discusses issues about graduate school, post doctoral positions, applying for faculty jobs and more.   The article also has some very good guidance for universities that would like to level the playing field:

We all know what structural changes would help to level the playing field in all of these careers and they are quite similar: paid family leave for both mothers and fathers, especially for childbirth, a flexible workplace, a flexible career track, a re-entry policy, pay equity reviews, child care assistance, dual career assistance. Those universities and corporations who have actively created these policies have found an advantage in recruitment and retention. For instance, at Berkeley, after enacting several new policies to benefit parents, including paid teaching leaves for fathers, job satisfaction scored much higher among parents, and more babies are being born to assistant professors.

Some good guidance for some of the activities at UC Davis as part of the ADVANCE program in which I am involved. And she ends by recommending

It is time for women to “lean in” and demand family policies that will at least give them a fighting chance to have both a successful career and babies.

I agree.  But it is also time for men to do the same.  The more that men also support and demand such policies the quicker things will change.

ADVANCE Reading of the Day: Sylvia Earle, Women in Japan and the Gulf, Spaceflight

Quick post here … Some news stories and posts I am checking out today in relation to the UC Davis ADVANCE project in which I am involved.

How Open Are You? Part 1: Metrics to Measure Openness and Free Availability of Publications

For many many years I have been raising a key questions in relation to open access publishing – how can we measure how open someone’s publications are.  Ideally we would have a way of measuring this in some sort of index.  A few years ago I looked around and asked around and did not find anything out there of obvious direct relevance to what I wanted so I started mapping out ways to do this.

When Aaron Swartz died I started drafting some ideas on this topic.  Here is what I wrote (in January 2013) but never posted:

With the death of Aaron Swartz on Friday there has been much talk of people posting their articles online (a short term solution) and moving more towards openaccess publishing (a long term solution).  One key component of the move to more openaccess publishing will be assessing people on just how good a job they are doing of sharing their academic work.

I have looked around the interwebs to see if there is some existing metric for this and I could not find one.  So I have decided to develop one – which I call the Swartz Openness Index (SOI).

Let A = # of objects being assessed (could be publications, data sets, software, or all of these together). 

Let B = # of objects that are released to the commons with a broad, open license. 

A simple (and simplistic) metric could be simply 

OI = B / A


This is a decent start but misses out on the degree of openness of different objects. So a more useful metric might be the one below.

A and B as above. 

Let C = # of objects available free of charge but not openly 

OI = ( B + (C/D) ) / A  

where D is the “penalty” for making material in C not openly available


This still seems not detailed enough.  A more detailed approach might be to weight diverse aspects of the openness of the objects.  Consider for example the “Open Access Spectrum.”  This has divided objects (publications in this case) into six categories in terms of potential openness: reader rights, reuse rights, copyrights, author posting rights, automatic posting, and machine readability.  And each of these is given different categories that assess the level of openness.  Seems like a useful parsing in ways.  Alas, since bizarrely the OAS is released under a somewhat restrictive CC BY-NC-ND  license I cannot technically make derivatives of it.  So I will not.  Mostly because I am pissed at PLoS and SPARC for releasing something in this way.  Inane.

But I can make my own openness spectrum.

And then I stopped writing because I was so pissed off at PLOS and SPARC for making something like this and then restricting it’s use.  I had a heated discussion with people from PLOS and SPARC about this but not sure if they updated their policy.  Regardless, the concept of an Openness Index of some kind fell out of my head after this buzzkill.  And it only just now came back to me. (Though I note – I did not find the Draft post I made until AFTER I wrote the rest of this post below … ).

To get some measure of openness in publications maybe a simple metric would be useful.  Something like the following

  • P = # of publications
  • A = # of fully open access papers
  • OI = Openness index

A simple OI would be

  • OI = 100 * A/P
However, one might want to account for relative levels of openness in this metric.  For example
  • AR = # of papers with a open but somewhat restricted license
  • F = # of papers that are freely available but not with an open license
  • C = some measure of how cheap the non freely available papers are
And so on.
Given that I am not into library science myself and not really familiar with playing around with this type of data I thought a much simpler metric would be to just go to Pubmed (which of course works only for publications in the arenas covered by Pubmed).
From Pubmed one can pull out some simple data. 
  • # of publications (for a person or Institution)
  • # of those publications in PubMed Central (a measure of free availability)
Thus one could easily measure the “Pubmed Central” index as
PMCI = 100 * (# publications in PMC / # of publications in Pubmed)
Some examples of the PMCI for various authors including some bigger names in my field, and some people I have worked with.
            Name                        #s                 PMCI    
Eisen JA
224/269  
83.2
Eisen MB 
76/104
73.1
Collins FS
192/521
36.8
Lander ES
160/377
42.4
Lipman DJ
58/73
79.4
Nussinov R
170/462
36.7
Mardis E
127/187
67.9
Colwell RR
237/435
54.5
Varmus H
165/408
40.4
Brown PO
164/234
70.1
Darling AE
20/27
74.0
Coop G
23/39
59.0
Salzberg SL
107/162
61.7
Venter JC
53/237
22.4
Ward NL
24/58
41.4
Fraser CM
78/262
29.8
Quackenbush J
95/225
42.2
Ghedin E
47/82
57.3
Langille MG
10/14
71.4

And so on.  Obviously this is of limited value / accuracy in many ways.  Many papers are freely available but not in Pubmed Central.  Many papers are not covered by Pubmed or Pubmed Central.  Times change, so some measure of recent publications might be better than measuring all publications.  Author identification is challenging (until systems like ORCID get more use).  And so on.

Another thing one can do with Pubmed is to identify papers with free full text available somewhere (not just in PMC).  This can be useful for cases where material is not put into PMC for some reason.  And then with a similar search one can narrow this to just the last five years.  As openaccess has become more common maybe some people have shifted to it more and more over time (I have — so this search should give me a better index).

Lets call the % of publications with free full text somewhere the “Free Index” or FI.  Here are the values for the same authors.

Name
PMC 
%
Pudmed 
PMCI 
Free
%
Pubmed
5 years
FI – 5 
Free
%
Pubmed
All
FI-ALL
Eisen JA
224/269
83.2
178/180
98.9
237
88.1
Eisen MB 
76/104
73.1
32/34
94.1
83 79.8
Collins FS
192/521
36.8
104/128
81.3
263 50.5
Lander ES
160/377
42.4
78/104
75.0
200 53.1
Lipman DJ
58/73
79.4
20/22
90.9
59 80.8
Mardis E
127/187
67.9
90/115
78.3
135 72.2
Colwell RR
237/435
54.5
31/63
49.2
258 59.3
Varmus H
165/408
40.4
21/28
75.0
206 50.5
Brown PO
164/234
70.1
20/21
95.2
185 79.0
Darling AE
20/27
74.0
18/21
85.7
21 77.8
Coop G
23/39
59.0
16/20
80.0
28 71.8
Salzberg SL
107/162
61.7
54/58
93.1
128 79.0
Venter JC
53/237
22.4
20/33
60.6
85 35.9
Ward NL
24/58
41.4
18/27
66.6
30 51.7
Fraser CM
78/262
29.8
9/13
69.2
109 41.6
Quackenbush J
95/225
42.2
54/75
72.0
131 58.2
Ghedin E
47/82
57.3
30/36
83.3
56 68.3
Langille MG
10/14
71.4
11/13
84.6
11 78.6

Very happy to see that I score very well for the last five years. 180 papers in Pubmed.  178 of them with free full text somewhere that Pubmed recognizes. The large number of publications comes mostly from genome reports in the open access journals Standards in Genomic Sciences and Genome Announcements.  But most of my non genome report papers are also freely available.

I think in general it would be very useful to have measures of the degree of openness.  And such metrics should take into account sharing of other material like data, methods, etc.  In a way this could be a form of the altmetric calculations going on.

But before going any further I decided to look again into what has been done in this area. When I first thought of doing this a few years ago I searched and asked around and did not see much of anything.  (Although I do remember someone out there – maybe Carl Bergstrom – saying there were some metrics that might be relevant – but can’t figure out who / what this information in the back of my head is).

So I decided to do some searching anew.  And lo and behold there was something directly relevant. There is a paper in the Journal of Librarianship and Scholarly Communication called: The Accessibility Quotient: A New Measure of Open Access.  By Mathew A. Willmott, Katharine H. Dunn, and Ellen Finnie Duranceau from MIT.

Full Citation: Willmott, MA, Dunn, KH, Duranceau, EF. (2012). The Accessibility Quotient: A New Measure of Open Access. Journal of Librarianship and Scholarly Communication 1(1):eP1025. http://dx.doi.org/10.7710/2162-3309.1025
Here is the abstract:

Abstract
INTRODUCTION The Accessibility Quotient (AQ), a new measure for assisting authors and librarians in assessing and characterizing the degree of accessibility for a group of papers, is proposed and described. The AQ offers a concise measure that assesses the accessibility of peer-reviewed research produced by an individual or group, by incorporating data on open availability to readers worldwide, the degree of financial barrier to access, and journal quality. The paper reports on the context for developing this measure, how the AQ is calculated, how it can be used in faculty outreach, and why it is a useful lens to use in assessing progress towards more open access to research.
METHODS Journal articles published in 2009 and 2010 by faculty members from one department in each of MIT’s five schools were examined. The AQ was calculated using economist Ted Bergstrom’s Relative Price Index to assess affordability and quality, and data from SHERPA/RoMEO to assess the right to share the peer-reviewed version of an article.
RESULTS The results show that 2009 and 2010 publications by the Media Lab and Physics have the potential to be more open than those of Sloan (Management), Mechanical Engineering, and Linguistics & Philosophy.
DISCUSSION Appropriate interpretation and applications of the AQ are discussed and some limitations of the measure are examined, with suggestions for future studies which may improve the accuracy and relevance of the AQ.
CONCLUSION The AQ offers a concise assessment of accessibility for authors, departments, disciplines, or universities who wish to characterize or understand the degree of access to their research output, capturing additional dimensions of accessibility that matter to faculty.

I completely love it.  After all. it is directly related to what I have been thinking about and, well, they actually did some systematic analysis of their metrics.  I hope more things like this come out and are readily available for anyone to calculate.  Just how open someone is could be yet another metric used to evaluate them …

And then I did a little more searching and found the following which also seem directly relevant

So – it is good to see various people working on such metrics.  And I hope there are more and more.
Anyway – I know this is a bit incomplete but I simply do not have time right now to turn this into a full study or paper and I wanted to get these ideas out there.  I hope someone finds them useful …

Another week – another microbial art project

The use of microbes in art projects continues to spread.  Here is another example: Bioluminescent art: Beautiful bacteria glow in the dark | MNN – Mother Nature Network.  The article discusses the Bioglyphs project which involved “some microbiology training, imagination, and a lot of petri dishes.”  Definitely worth checking out …

ADVANCE Journal Club: Developing Graduate Students of Color for the Professoriate in STEM

As I have posted about before – I am involved in the UC Davis ADVANCE project funded by NSF.  From the project website:

UC Davis ADVANCE is a newly funded Institutional Transformation grant that began in September of 2012. Our program is supported by the National Science Foundation’s ADVANCE Program which aims to increase the participation and advancement of women in academic science and engineering careers. 

My role in this project is as a member (and now Co-Chair) of one of the “Policies and Practices Review Initiative” Committee.  As part of my work on this committee I am trying to read various papers on related topics.  And I figured I would simultaneously post about these papers as much as I can because it would be great to get a broader discussion going on these topics.

So today I am reading the following:CSHE – Developing Graduate Students of Color for the Professoriate in Science, Technology, Engineering, and Mathematics (STEM) which I was pointed to in our Committee meeting yesterday.  It is quite interesting.  It is by Anne MacLachlan from the Center for Studies in Higher Education at UC Berkeley.

The abstract:

This paper presents part of the results of a completed study entitled A Longitudinal Study of Minority Ph.D.s from 1980-1990: Progress and Outcomes in Science and Engineering at the University of California during Graduate School and Professional Life. It focuses particularly on the graduate school experience and degree of preparation for the professoriate of African American doctoral students in the sciences and engineering, and presents the results of a survey of 33 African American STEM Ph.D.s from the University of California earned between 1980-1990. Relationships with thesis advisors and principal investigators are evaluated by the study participants in fifteen specific areas from highly-ranked intellectual development to low-ranked training in grant writing. Deficits in training and socialization are discussed along with the tension between being both an African American and a graduate student. Career choices and outcomes are presented. These findings, in conjunction with current analyses of graduate education in STEM, suggest ways in which graduate training for all could be improved.

Lots of interesting information in there.  Perhaps most important for my current goals is what she describes at the end in terms of a Proposed Development Program.  She starts this section by commenting on the general situation in terms of training scientists in the US today.  She then identifies what she refers to a “discontinuities” in federal and local policy which can hinder “developing faculty of color.”  These include “compartmentalized, externally mandated sets of programs” and the “nature of Ph.D. training”.  Of the 33 Ph.D.s surveyed in the study, nearly all of them recommended diversity training for faculty.  They also recommend better laying out of expectations and requirements for students and more involvement of current faculty in recruiting.  They also made many recommendations for improving the life of current students of color.

Anyway – a lot of this material and the concepts involved are bit new to me so I am still digesting the article.  But I thought I would share it with others in the hope that this will help catalyze more open discussion of issues involved women and underrepresented minorities in STEM fields.

Weird things coming up from automated Google Scholar searches pointing to hea1thandfitness.com

I noticed some really weird stuff coming up in automated Google Scholar searches.  Example – see this one below:

Scholar Alert: [ metagenomics phylogeny ]

[HTML] Asthma and the Diversity of Fungal Spores in Air

A Pringle – PLoS Pathogens, 2013
 cause and effect between spores and asthma may remain a challenge, metagenomictechnologies
will  Metagenomics data are likely to provide a very different understanding of the potential diversity 
(2006) Reconstructing the early evolution of fungi using a six-gene phylogeny


[HTML] Insights inside often the progression amongst Archaea additionally eukaryotic required protein modifier metabolism exposed simply because amongst often the …

T Nunoura, Y Takaki, J Kakuta, S Nishi, J Sugahara… – Life Sciences
 ‘ ‘, gives become proposed centred on SSU rRNA gene phylogeny (10 ), unfortunately a type II
SSU rRNA gene set identified on the metagenomic library; AB566230.  Archaea: sides ranging
from microbial ecology and regarding consequence metagenomics GarrettRA KlenkH-P 

The second paper listed there takes one to a very strange site. It appears to be a pseudo-mirror of the journal site all embedded within the domain “Hea1thandFitness.Com”.  Note – this domain name has the number “1” replacing the letter “l” in the domain name – I assume as a trick of sorts.  Clicking on the link takes you to a site for which I have done a screen shot below


The whole thing is weird – with the number instead of the letter and the weird formatting of the site.  Just a tiny glitch?  Well, I don’t think so since in some of my other Google Scholar alerts other links to this same domain came up.  See examples below:

Scholar Alert: New articles in Phil Hugenholtz’s profile

[HTML] Contrasting Life Strategies involving Viruses that’s Infect Photo-certainly to positively not mention Heterotrophic Bacteria, considering that’s Revealed by simply Viral …

L Deng, A Gregory, S Yilmaz, BT Poulos, P Hugenholtz…
Ocean infections are usually all-pervasive and also numerous and also play the game main
jobs relating to be the inside overseas biogeochemical menstrual cycles thru their mortality,
horizontally gene transfer, and also mind games about put in relationship metabolism. 

and

Scholar Alert: [ PhylogenoMics ]

[HTML] PIECE: a collection to help your entire family take also gene rules comparing and then progression

Y Wang, FM You, GR Lazo, MC Luo, R Thilmony… – Life Sciences
 structural repair for retrogenes appearing in the organization for the Populus genome 2009 151
1943 1951 AbstractFREE Full Text Garcia-Espana Mares SunTT Desalle Intron evolution: checking
hypotheses for intron development by consuming phylogenomics for tetraspanins 

[HTML] Integration of sequence-similarity and therefore practical union information definitely likely surmounted inbuilt factors found in orthology mapping through bacterial …

G Li, Q Ma, X Mao, Y Yin, X Zhu, Y Xu – Life Sciences
 Chen MackeyAJ VermuntJK RoosDS Assessing entire performance of orthology discovery
strategies put to practice found on eukaryotic genomes 2007 e383 CrossRef Medline ZmasekCM
EddySR RIO: analyzing proteomes by automated phylogenomics wearing resampled 


and

Scholar Alert: [ microbial forensics ]

Effect of modified montmorillonites on the biodegradation and adsorption of biomarkers such as hopanes, steranes and diasteranes

UC Ugochukwu, IM Head, DAC Manning – 2013
 Several studies have demonstrated that some solid sur- faces such as clay minerals are able
to stimulate microbial  Indigenous microbial cells of Whitley Bay sediments were iso- lated and
proliferated via several subcultures prior to use for laboratory biodegradation studies. 

[HTML] Deconstruction created by Lignocellulose interested in Soluble Sugars by the Native and even Designer Cellulosomes

S Moraïs, E Morag, Y Barak, D Goldman, Y Hadar…
 be in charge created by for the focusing on sense made out created by the comprehensive
forensics education a  Previous SectionNext Section Designer cellulosome technology also has
also been recommended to your indigenous microbial enzymatic destruction created by 

[HTML] Molecular multiplying associated with polymerases for resistor to environmental inhibitors

C Baar, M d’Abbadie, A Vaisman, ME Arana… – Life Sciences
 associated with plans in medicine and biology running ranging from analysis and diagnostics,
prognostics, forensics to molecular  using the QiaAmp DNA miniature apparatus (Qiagen) being
for each and every manufacturer’s instructions, upcoming microbial standard protocol C 


So incredibly weird. Is there some site out there that figured out how to scam Google Scholar into linking to them? Anyone seen anything like this before?

Yes, microbes are likely important everywhere, but evidence would be nice (re Atlantic piece on Soil)

Just read this article in the Atlantic: Healthy Soil Bacteria, Healthy People – Mike Amaranthus & Bruce Allyn – The Atlantic.  It is interesting in a few ways.  But what got me a bit up in arms about it is the number of statements and claims that are not backed up by any reference to evidence.  Consider the following:

“Just as we have unwittingly destroyed vital microbes in the human gut through overuse of antibiotics and highly processed foods, we have recklessly devastated soil microbiota essential to plant health through overuse of certain chemical fertilizers, fungicides, herbicides, pesticides, failure to add sufficient organic matter (upon which they feed), and heavy tillage.”

OK – sounds serious.  But is it really true?  Have pesticides really devastated soil microbiota?  What about tillage?  Seems possible, but also seems possible that this would not be true.  Would be nice to see the evidence behind this claim.

How about this one:

“Reintroducing the right bacteria and fungi to facilitate the dark fermentation process in depleted and sterile soils is analogous to eating yogurt (or taking those targeted probiotic “drugs of the future”) to restore the right microbiota deep in your digestive tract.”

Sounds good too.  But way too overly simplistic.  I mean – probiotics for people are a bit of a complicated mess right now.  Some work.  Most probably don’t.  Most of the claims are overblown.  So to say we know how to do this well in “soil” definitely seems to be an overstatement.  Again, specific evidence for this would be nice.

And then this:

“Due to new genetic sequencing and production technologies, we have now come to a point where we can effectively and at low cost identify and grow key bacteria and the right species of fungi and apply them in large-scale agriculture.”

Soil is a very very complicated place in terms of microbes.  I personally think we are really far away from this utopian view of growing the key species to apply them to large scale ag.  Evidence that this is true?  I don’t know of much.  Yes we can sequence things.  We can sequence a lot of things.  But “identify and grow key bacteria and the right species of fungi” – I think we are far from being able to do this robustly.

Another claim in the article has some ring of truth:

We can sow the “seeds” of microorganisms with our crop seeds and, as hundreds of independent studies confirm, increase our crop yields and reduce the need for irrigation and chemical fertilizers.

Yes, this has a ring of truth.  Certainly there are studies – many of them – involving adding microbes to seeds and how that impacts yield and nutrient and water requirements.  And without a doubt in many cases such inoculation can help in many ways.  But the “hundreds of independent studies” claim is a bit misleading as there are also many cases where inoculation does not help.  So we should be cautious before adding microbes to seeds becomes the equivalent of probiotics for people.   Not all probiotics that are claimed to help people actually do anything.  And not all microbes added to seeds will do much of anything useful either.

How about the claim:

Thus the microbial community in the soil, like in the human biome, provides “invasion resistance” services to its symbiotic partner. We disturb this association at our peril

Sounds good.  And has a ring of truth too.  And in general I agree with the sentiment that we should not screw with ecosystems without recognizing that the microbes in those systems may play important and useful roles.  However, just because SOME microbes play important and useful roles in systems does not of course mean that ALL are ones we want to keep.  There will be some in the soil that damage plants and hurt yield and pathogen resistance just as there will be some that are “good” from our point of view.

And then there is this

We are now at a point where microbes that thrive in healthy soil have been largely rendered inactive or eliminated in most commercial agricultural lands; they are unable to do what they have done for hundreds of millions of years, to access, conserve, and cycle nutrients and water for plants and regulate the climate. 

And also

The mass destruction of soil microorganisms began with technological advances in the early twentieth century. 

Sounds nice.  But I don’t really know of much evidence that the microbes have been rendered inactive or eliminated in commercial agricultural lands.

I suppose this is all building up to the following

Fortunately, there is now a strong business case for the reintroduction of soil microorganisms in both small farms and large-scale agribusiness. Scientific advances have now allowed us to take soil organisms from an eco-farming niche to mainstream agribusiness. We can replenish the soil and save billions of dollars.

and

For all these reasons, bio fertility products are now a $500 million industry and growing fast. The major agricultural chemical companies, like Bayer, BASF, Novozymes, Pioneer, and Syngenta are now actively selling, acquiring or developing these products.

So — this is in a way an article promoting the financial benefit of adding microbes to soil.  I think this is reasonable although not completely convincing.  Alas, after reading the article I discovered this about one of the authors

Mike Amaranthus is the chief scientist at Mycorrhizal Applications, Inc., a company working on innovations in soil biology. 

This is not to say that someone with a financial role in convincing the world to add microbes to soil cannot be trusted to provide a good guide about microbes in the soil.  But it would have been nice for this to be mentioned more prominently in the article.  Many of the claims in this article do not pass the smell test to me.  And all of them seem to be pointing towards a solution involving a company that one of the authors is involved in.  If this were about human medical treatments many many people might get bent out of shape by this.  Again, not to say people with financial interests cannot write good articles.  But the potential for conflicts in such cases, as in the case here, is great.  And thus we should view with a tint of extra skepticism some of the claims made by such individuals.  And in this case here I already felt uncomfortable with many of the claims.  I think the Atlantic could do better and could certainly require the author to make more clear in the article itself  what the author’s personal interest in the claims are.

Fall 2013 Graduate Course in Applied Ecological Genetics: ECL242 / PHR242

Thought this might be of interest

 

Dynamic graduate level course in ecological genetics offered Fall 2013 at UC Davis.

Applied Ecological Genetics:
Genetics and Genomics for Ecology, Health, and Conservation of Natural Populations

Making genetics friendly and accessible.
This course is an introductory course to the topic for graduate students…and yet packed with great information.

REGISTRATION INFO:
Ecology and Pop Bio grad students sign up for ECL242 CRN 29983
Grad students in all other grad groups sign up for PHR242 CRN 46002 

3 units
10:00-11:50 Wed and Fridays Fall quarter 2013
Instructor: Holly Ernest

For graduate students in any graduate group interested in applications of genetics/genomics for ecology, conservation biology, and natural systems management.  Space as available for post-docs, project scientists, and others.

More info:  http://www.vetmed.ucdavis.edu/vgl/wildlife/Ecological_Genetics_Course.html

Great course for students interested in:
• building skills and knowledge to develop the best questions and approaches for ecological genetic and genomics projects
• gaining knowledge in ecological and conservation genetics/genomics for a career in wildlife and natural resource agencies, nonprofit organizations, and academic institutions.  Genetics and genomics is increasingly a key conservation tool.
• evaluating published genetic analyses for ecological questions and management applications.
• applicable to fields including, but not limited to, conservation ecology, population biology, wildlife health, disease ecology, avian science, plant biology, anthropology, entomology, veterinary medicine, and others.

Objectives: 

1. Students will gain understanding of the scope and breadth of genetic/genomic applications for research and applications in ecology, conservation management, and wildlife population health.
2. Students will become familiar with concepts of laboratory and computational techniques commonly used for ecological genetics research.
3. Students will become familiar with key theory underlying genetic data analysis for ecology.
4. Students will gain knowledge and skills in development of well-designed questions, hypotheses and research projects, basic data analysis techniques, and problem-solving in the field of ecological genetics.

Topics
• Sampling techniques and strategies
• Molecular markers and lab techniques: including next generation sequencing, whole genome, microsatellites, mitochondrial DNA, etc
• Data analysis
• Study design
• Genetics of endangered species; invasive species
• Introductory material for Ecological genomics – future courses will be offered by Ecology faculty in this area.  ECL242 will help set the foundation for the more advanced genomics courses.
…and much more! … covered in lecture, computer lab, and discussion

Special Guest speakers and sessions tentatively on schedule
• Computer lab sessions: intro to computational aspects of work with genetic data, genotypic data, sequence data;
• Genome research specialists lined up to tell us about: genomics of wild ancestors of crop plants, insects that are key disease vectors, polyploid fish, birds of conservation concern, endangered mammals, genomics and ecotoxicology, etc
• UCD Genome Center talk and tour

Note that this course will likely be one of the core courses for Ecology Grad Group’s proposed new Area of Emphasis (AOE) in Ecological Genetics and Genomics

Important read for those interested in gender, family & academia: Do Babies Matter

Just got pointed to this by Julie Huber on Facebook: New book on gender, family and academe shows how kids affect careers in higher education | Inside Higher Ed.  The book is “Do Babies Matter? Gender and Family in the Ivory Tower.”  This looks like a very important book and is especially relevant to me in my role in the UC Davis ADVANCE project where we are working on related issues.  It is from Mary Ann Mason at Berkeley Law School, Nicholas Wolfinger from Utah, and Marc Goulden from the UC Berkeley Office for Faculty Equity and Welfare.  It is definitely worth checking out.

I am ordering it right now …

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6/12 at #UCDavis: Stephen Scherer on “Detection of Clinically Relevant Genetic Variants in Autism Spectrum”

UC Davis MIND Institute’s 2012-2013 Distinguished Lecturer Series

SPEAKER: Stephen Scherer, PhD, DSc
TOPIC:
Detection of Clinically Relevant Genetic Variants in Autism Spectrum Disorder
DATE:
Wednesday, June 12, 2013
TIME: 4:30 pm – 6:00 pm
LOCATION:
MIND Institute Auditorium (2825 50th Street, Sacramento)

Background Information ( see attached and below)

Bio Info: Stephen Scherer, PhD, DSc, FRSC, holds the GlaxoSmithKline-Canadian Institutes of Health Research Endowed Chair in Genome Sciences at The Hospital for Sick Children and University of Toronto. Dr. Scherer is director of the University of Toronto’s McLaughlin Centre and The Centre for Applied Genomics. He has made numerous contributions to medical genetics including mapping, sequencing and disease gene studies of human chromosome 7. In 2004, his team co-discovered global gene copy number variation (CNV) and has since shown that CNV is the most abundant type of genetic variation of human DNA. His group then identified CNV that contribute to the etiology of autism and many other disorders. The Database of Genomic Variants that he founded facilitates hundreds of thousands of clinical diagnoses each year. His work is documented in over 300 publications and patents and cited more than 20,000 times, ranking him as one of the top cited scientists over the past decade worldwide. Dr. Scherer has won numerous honors such as the 2004 Steacie Prize, an International Howard Hughes Medical Institute Scholarship, and the Premiers Summit Award for Medical Research. He is a distinguished Fellow of the Canadian Institute for Advanced Research, the American Association for the Advancement of Science, and the Royal Society of Canada.

Presentation: (Detection of Clinically Relevant Genetic Variants in Autism Spectrum Disorder )
Autism Spectrum Disorder (ASD) demonstrates high heritability, familial clustering and ~4:1 male to female bias, yet the causes are only partially understood, due to extensive clinical and genetic heterogeneity. Whole genome sequencing (WGS) promises added value to identify novel ASD risk genes, as well as new mutations in known loci, but an assessment of its full utility in an ASD group has not been performed. In a pilot study, we used WGS to examine 32 families with ASD to detect de novo or rare inherited genetic variants predicted to be deleterious (loss-of-function and damaging missense mutations). Among ASD probands, we identified deleterious de novo mutations in 6 of 32 (19%) and X-linked or autosomal inherited alterations in 10 of 32 (31%) families (some had combinations of mutations). The proportion of families identified with such mutations was larger than has been previously reported, a yield that is in part due to the more comprehensive coverage afforded by WGS. Deleterious mutations were found in four novel, 9 known, and 8 candidate ASD risk genes. Examples include CAPRIN1 and AFF2 (both linked to the FMR1 gene that is involved in fragile X syndrome), VIP (involved in social-cognitive deficits), and other genes such as SCN2A and KCNQ2 (also linked to epilepsy), NRXN1, and CHD7, which causes ASD-associated CHARGE syndrome. Taken together, these results suggest that WGS and thorough informatic analyses may improve the detection of genetic variants likely associated with ASD or its associated clinical symptoms

Scherer_ Bioabstract_05282013.pdf