2 Matching Annotations
- Sep 2021
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www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
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To identify early embryonic base substitutions, we analysed whole-genome sequences of blood samples from 279 individuals with breast cancer (mean sequencing coverage 32-fold; Supplementary Table 1) seeking mutations with VAFs ranging from 10% to 35%
This is what the research is studying.
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- Sep 2017
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www.biorxiv.org www.biorxiv.org
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Major flaws in "Identification of individuals by trait prediction using whole-genome sequencing data"
re Venter study in PNAS, claiming to be able to identify people based on whole genome data
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