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Hakenberg et al., 2016 - Google Patents

Integrating 400 million variants from 80,000 human samples with extensive annotations: towards a knowledge base to analyze disease cohorts

Hakenberg et al., 2016

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Document ID
4929018429983807689
Author
Hakenberg J
Cheng W
Thomas P
Wang Y
Uzilov A
Chen R
Publication year
Publication venue
BMC bioinformatics

External Links

Snippet

Background Data from a plethora of high-throughput sequencing studies is readily available to researchers, providing genetic variants detected in a variety of healthy and disease populations. While each individual cohort helps gain insights into polymorphic and disease …
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