Most Recent Year Journal Club

2008-2009

2008-2009

Tuesday, September 30, 2008 03:00PM Crossroads, Community Lounge

Presenter:Matt Zawistowski
Common and rare variants in multifactorial susceptibility to common diseases.
    Nat Genet (2008) 40:695-701. Bodmer W, Bonilla C.
URL:http://www.nature.com/ng/journal/v40/n6/abs/ng.f.136.html

Tuesday, October 14, 2008 04:00PM SPH Crossroads, Community Lounge

Presenter:Shyam Gopalakrishnan
Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data.
    AJHG. 2008 83:311-21. Li B, Leal SM.
URL:http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B8JDD-4T5BRBT-1-2&_cdi=43612&_user=99318&_coverDate=09%2F12%2F2008&_sk=%23TOC%2343612%232008%23999169996%23697622%23FLA%23display%23Volume_83,_Issue_3,_Pages_297-430_(12_September_2008)%23tagged%23Vo

Tuesday, October 28, 2008 03:00PM SPH II Rm M1122

Presenter:Tanya Teslovich
Multiple rare variants in NPC1L1 associated with reduced sterol absorption and plasma low-density lipoprotein levels.
    Proc Natl Acad Sci U S A. 2006 103:1810-5. Cohen JC, Pertsemlidis A, Fahmi S, Esmail S, Vega GL, Grundy SM, Hobbs HH.
URL:http://www.pubmedcentral.nih.gov/picrender.fcgi?artid=1413637&blobtype=pdf

Tuesday, November 18, 2008 TBA

Presenter:NA
ASHG Summary
    TBA
URL:http://TBA

Tuesday, January 27, 2009 03:00PM SPH II CR 2610

Presenter:Steve Qin
Accurate whole human genome sequencing using reversible terminator chemistry.
    Nature (2008) 456:49-51. Bentley DR et al.
URL:http://www.nature.com.proxy.lib.umich.edu/nature/journal/v456/n7218/pdf/nature07517.pdf

Thursday, February 19, 2009 03:00PM SPH II CR 2610

Presenter:Jun Ding
Mapping of Expression-QTLs Yields Insight into Human Gene High-Resolution Regulation.
    (2008) PLoS Genet 4: e1000214. doi:10.1371/journal.pgen.1000214, Veyrieras J-B, Kudaravalli S, Kim SY, Dermitzakis ET, Gilad Y, et al.
URL:http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1000214

Tuesday, March 03, 2009 03:00PM 2610 CR SPH

Presenter:Ming Hu
High-resolution mapping of copy-number alterations with massively parallel sequencing.
    Nat Methods. 2009 Jan;6(1):99-103. Chiang DY, Getz G, Jaffe DB, O'Kelly MJ, Zhao X, Carter SL, Russ C, Nusbaum C, Meyerson M, Lander ES.
URL:http://NA

Tuesday, March 17, 2009 03:00PM 2610 CR SPH

Presenter:Jun Li
A technical appraisal of RNASeq
    N/A
URL:http://N/A

Tuesday, March 31, 2009 03:00PM CR 2610, SPH

Presenter:Ryan Welch
Pathway analysis of seven common diseases assessed by genome-wide association.
    Genomics 2008, 92:265-272. Torkamani A, Topol EJ, Schork NJ.
URL:http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6WG1-4TFV91X-2&_user=99318&_coverDate=11%2F30%2F2008&_alid=893193928&_rdoc=20&_fmt=high&_orig=search&_cdi=6809&_sort=d&_docanchor=&view=c&_ct=69&_acct=C000007678&_version=1&_urlVersion=0&_userid=99

Tuesday, April 14, 2009 03:00PM 2610 Crossroads SPH

Presenter:Wei Chen
Mapping short DNA sequencing reads and calling variants using mapping quality scores.
    Genome Res. 2008 18: 1851-1858. Li H, Ruan J, Durbin R.
URL:http://genome.cshlp.org.proxy.lib.umich.edu/content/18/11/1851.full.pdf+html?sid=b2be965b-4668-43d8-876d-3b59091a1ab6

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