Posts Tagged ‘#genomics’

Patients’ Genes Seen as Future of Cancer Care – NYTimes.com

April 23, 2013

http://www.nytimes.com/2013/04/22/health/patients-genes-seen-as-future-of-cancer-care.html

Relating CNVs to transcriptome data at fine resolution: Assessment of the effect of variant size, type, and overlap with functional regions

April 19, 2013

http://genome.cshlp.org/content/21/12/2004.long
initial cnv eqtls

From pseudogenes to proteins

April 19, 2013

Gencode perspective on massspec of pseudogenes
http://www.nature.com/nmeth/journal/v8/n6/full/nmeth0611-448b.html

Identifiability Think Tank Report Published in Genetics in Medicine

April 12, 2013

an article describing the Think Tank was just published online in Genetics in Medicine:
http://www.nature.com/doifinder/10.1038/gim.2013.40

Somatic evolutionary genomics: Mutations during development cause highly variable genetic mosaicism with risk of cancer and neurodegeneration

April 9, 2013

Paper giving a conceptual framework to somatic mosaicism

http://www.pnas.org/content/107/suppl.1/1725.full

Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array

March 31, 2013

http://www.nature.com/ng/journal/v45/n4/full/ng.2560.html?WT.ec_id=NG-201304

Retrotransposition of gene transcripts leads to structural variation in mammalian genomes

March 17, 2013

Adam D Ewing, Tracy J Ballinger, Dent Earl, Broad Institute Genome Sequencing and Analysis Program, Christopher C Harris, Li Ding, Richard K Wilson and David Haussler

http://genomebiology.com/2013/14/3/R22/abstract

Absolute quantification of somatic DNA alterations in human cancer

March 17, 2013

Nat Biotechnol. 2012 May;30(5):413-21. doi: 10.1038/nbt.2203. Carter SL, Cibulskis K, Helman E, McKenna A, Shen H, Zack T, Laird PW, Onofrio RC, Winckler W, Weir BA, Beroukhim R, Pellman D, Levine DA, Lander ES, Meyerson M, Getz G.

Cell – Identifying Recent Adaptations in Large-Scale Genomic Data

March 9, 2013

pos. sel. from 1000G phase 1

http://www.cell.com/retrieve/pii/S0092867413000871
Cell, Volume 152, Issue 4, 703-713, 14 February 2013
Copyright © 2013 Elsevier Inc. All rights reserved.
10.1016/j.cell.2013.01.035
Sharon R. Grossman,Kristian G. Andersen,Ilya Shlyakhter,Shervin Tabrizi,Sarah Winnicki,Angela Yen,Daniel J. Park,Dustin
Griesemer,Elinor K. Karlsson,Sunny H. Wong,Moran Cabili,Richard A. Adegbola,Rameshwar N.K. Bamezai,Adrian V.S. Hill,Fredrik O.
Vannberg,John L. Rinn,1000 Genomes Project,Eric S. Lander,Stephen F. Schaffner,Pardis C. Sabeti

RNA studies under fire

March 7, 2013

High-profile results challenged over statistical analysis of sequence data http://www.nature.com/news/rna-studies-under-fire-1.10502

“In July 2010, a team led by Catherine Dulac and Christopher Gregg, both then at Harvard University in Cambridge, Massachusetts, published a study in Science estimating that 1,300 mouse genes — an order of magnitude more than previously known — were imprinted.
Now, researchers are arguing that a flawed analysis led Dulac and Gregg to vastly over­estimate imprinting in their paper.”