Shilpa N. Kobren

Research Fellow @HarvardDBMI leveraging genome sequences with clinical data to derive insights on the molecular mechanisms underlying rare human diseases

[Isaac Kohane @zakkohane]

Timely warning how polygenic risk score risks can create pathological disparities in healthcare @NatureGenet https://t.co/d9Vrq33Ch9 with a reminder to increase diversity in population studies HT @IAmSamFin CC @arjunmanrai

[Isaac Kohane @zakkohane]

Great resource for finding protein domains interacting with DNA, RNA, peptides, ions or small molecules https://t.co/zgtC3MUbXT from @shilpanads formerly at Mona Singh’s lab @Princeton

[NIH Common Fund @NIH_CommonFund]

New funding opportunity to work with @UDNConnect uncovering biological mechanisms of genetic variants of interest. Learn more: https://t.co/aesXwfqLZU

[EPP @eppcan]

Here you can find a summary of our recent @CellCellPress paper about driver genes and mutations using #TCGA #PanCancerAtlas #AACR18 https://t.co/EEhm2cmTtp

[David Robinson @drob]

Wow- NLP analysis discovers more than a million fake anti-net-neutrality comments. Brilliant data science detective work by @thisismetis student Jeff Kao. https://t.co/p9vooF5GPd #datablog

[Broad Institute @broadinstitute]

Congrats to Broad Fellows Fei Chen, Hilary Finucane, and Ahmed Badran on receiving NIH Early Independence Awards! https://t.co/3fhL6JvynD