Posts Tagged ‘i0hgvs’

Variant impact prediction methods | Critical Assessment of Genome Interpretation

Sunday, October 22nd, 2017

https://genomeinterpretation.org/impact

Each name is scaled according to the logarithm of the number of citations. Colors are randomly assigned.

My public notes from #ASHG17 & its Satellites (#GenoPri17, #GA4GH2017, #HGVS17, idash, i0hgvs)

Sunday, October 22nd, 2017

Links

https://linkstream2.gerstein.info/tag/i0hgvs

Tweets

https://storify.com/markgerstein/favorite-tweets-from-ashg17-ga4gh2017-genopri17-hg

Talks

http://lectures.gersteinlab.org/summary/Mutations-in-2500-cancer-genomes–20171018-i0hgvs+ashg/

http://lectures.gersteinlab.org/summary/Prioritizing-somatic-variants–20171017-i0hgvs+main/

http://lectures.gersteinlab.org/summary/Genomic-Privacy-n-RNAseq-Quantifying-Leakage–20171014-i0hgvs+idash/

Pics

https://www.flickr.com/photos/tags/seriesi0hgvs

Blinkist vs. Wikipedia: What’s the Best Way to Cram-Read? – The Atlantic

Saturday, October 21st, 2017

Blinkist vs. Wikipedia: What’s the Best Way to Cram-Read? – The Atlantic

https://www.theatlantic.com/technology/archive/2015/11/please-be-brief/417894/

KanbanFlow – Lean project management. Simplified.

Saturday, October 21st, 2017

https://kanbanflow.com/

German activities on RNA privacy

Saturday, October 21st, 2017

http://www.mhumbert.com/publications/oakland17.pdf

Identifying Personal DNA Methylation Profiles by Genotype Inference

Michael Backes⇤, Pascal Berrang⇤, Matthias Bieg†, Roland Eils†‡, Carl Herrmann†‡, Mathias Humbert⇤, Irina Lehmann§

Re-Identification of Individuals in Genomic Data-Sharing Beacons via Allele Inference | bioRxiv

Saturday, October 21st, 2017

https://www.biorxiv.org/content/early/2017/10/09/200147
higher order markov to predict snps

U.S. Department of Health & Human Services – Office for Civil Rights

Saturday, October 21st, 2017

list of breaches

https://ocrportal.hhs.gov/ocr/breach/breach_report.jsf

Lifetimes of cryptographic hash functions

Saturday, October 21st, 2017

http://valerieaurora.org/hash.html

Haplotype-based profiling of subtle allelic imbalance with SNP arrays

Saturday, October 21st, 2017

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3530675/

Discovering novel pharmacogenomic biomarkers by imputing drug response in cancer patients from large genomics studies

Saturday, October 21st, 2017

Geeleher cites http://genome.CSHLP.org/content/early/2017/08/28/gr.221077.117?top=1 … Novel pharmacogenomic biomarkers by imputing drug response in cancer..from…genomics studies #ASHG17
http://genome.cshlp.org/content/early/2017/08/28/gr.221077.117?top=1