Posts Tagged ‘#gi2017’

Genome Informatics meeting

Monday, November 6th, 2017

LINKS

https://linkstream2.gerstein.info/tag/i0gi2017/

TWEETS

https://storify.com/markgerstein/favorite-tweets-from-genome-informatics-17-gi2017-

TALK

http://lectures.gersteinlab.org/summary/Mutations-in-2500-cancer-genomes–20171104-i0gi2017/

OTHER materials (passwd access) in
http://meetings.gersteinlab.org/2017/10.28/i0gi2017/

DMDM: domain mapping of disease mutations | Bioinformatics | Oxford Academic

Sunday, November 5th, 2017

https://academic.oup.com/bioinformatics/article/26/19/2458/229387

Links to “Oncology at the Limits” and TRACERx Consortium

Sunday, November 5th, 2017


Here is a link to the “Oncology at the Limits” Conference which is co-organised between UCL and Yale, …. It will be from
19th to 21st March at the Royal College of Physicians in London.

http://www.thelancet.com/education/at-the-limits/oncology-2017

https://www.atthelimits.org/

The Keynote this year was … about the Lung TRACERx consortium. It is a project which
performs multi-site sampling of tumours to gain an insight into subclonal populations, and also follows up on the presence, expansion or response to therapy of these subclones via circulating-tumour-DNA. …

http://www.thelancet.com/education/at-the-limits/oncology-2017/sequencing-cancer-genomes-and-personalising-cancer-treatments

….

Split Sequence Bloom Trees – Kingsford Group

Sunday, November 5th, 2017

http://kingsfordlab.cbd.cmu.edu/2016/12/18/split-sequence-bloom-trees/

Fast search of thousands of short-read sequencing experiments : Nature Biotechnology : Nature Research

Sunday, November 5th, 2017

https://www.nature.com/nbt/journal/v34/n3/full/nbt.3442.html

GitHub – ryanlayer/stix: Structural Variant Index

Sunday, November 5th, 2017

https://github.com/ryanlayer/stix

BioData18

Sunday, November 5th, 2017

7 to 10 Nov. 2018

biological data sci ’18

https://meetings.cshl.edu/meetings.aspx?meet=DATA&year=18

BioViz – Home

Sunday, November 5th, 2017

http://bioviz.org/igb/

SEQSpark: A Complete Analysis Tool for Large-Scale Rare Variant Association Studies Using Whole-Genome and Exome Sequence Data: The American Journal of Human Genetics

Sunday, November 5th, 2017

http://www.cell.com/ajhg/fulltext/S0002-9297(17)30235-5

Advgenemap2018 – Center for Statistical Genetics

Sunday, November 5th, 2017

https://statgen.research.bcm.edu/index.php/Advgenemap2018

statgen.research.bcm.edu/advgenemap2018/view