Posts Tagged ‘sb’

Circle of life

Saturday, November 15th, 2014

the "circle of life"

Volume 24, Issue 6, pR238–R240, 17 March 2014

Evolution: Dynamics of De Novo Gene Emergence

Rafik Neme
Diethard Tautz


Adzhubei IA, Schmidt S, Peshkin L, Ramensky VE, Gerasimova A, Bork P, Kondrashov AS, Sunyaev SR. A method and server for predicting damaging missense mutations. Nature Methods (2010) 7: 248-249.

Saturday, October 11th, 2014

Server for predicting damaging missense #mutations Polyphen2 uses both structure & sequence (eg ASA & conservation)

Polyphen2 includes both structural and sequence features to predict the effect of nonsynonymous substitutions on protein function. Similar to many other methods, Polyphen2 uses evolutionary conservation as one of the features to identify functionally important residues. Integration of 3D-structure, membrane-specific features (PHAT matrix for TM regions) and other features such as protein-domain and active-site are the strengths of Polyphen2 compared to other sequence-based software making it a good tool for prediction.

Realizing the promise of cancer predisposition genes : Nature : Nature Publishing Group

Friday, September 19th, 2014

cell free DNA circulating for cancer

Monday, May 12th, 2014

NYT recently ran an article as well:

An ultrasensitive method for quantitating circulating tumor DNA with broad patient coverage
DIAGNOSTICS: Detection of Chromosomal Alterations in the Circulation of Cancer Patients with Whole-Genome Sequencing

Another VAT!

Friday, May 9th, 2014

Variant Association Tools for Quality Control and Analysis of Large-Scale Sequence and Genotyping Array Data


Processed pseudogenes acquired somatically during cancer development

Saturday, April 12th, 2014

age distribution of repeats

Monday, March 24th, 2014

From the following article:
Initial sequencing and analysis of the human genome
International Human Genome Sequencing Consortium
Nature 409, 860-921(15 February 2001)

Alu age distribution

NA12878 high confidence calls

Thursday, February 20th, 2014

Integrating genotype from many callers & indication of where they differ. Might be useful for the personal diploid genome.

classification of genomics researchers

Sunday, January 19th, 2014

Ten recommendations for creating usable bioinformatics command line software

Sunday, January 19th, 2014