NA12878 associated_with 1000 Genomes Project
Evidence from:
primary |
all sources
Evidence (3 sources)
Statistical modeling for sensitive detection of low-frequency single nucleotide variants.
(2016)
PMID:27556804
primary
tumor sample is a mixture of 17 individuals from 1000 Genomics Project plus NA12878
confidence: 0.95
Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples.
(2013)
PMID:23396013
cited
deep-coverage data from a high coverage whole-genome sample (NA12878) sequenced ... by the 1000 Genomes Project
confidence: 0.95
Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples.
(2013)
PMID:23396013
cited
NA12878 ... sequenced ... by the 1000 Genomes Project
confidence: 0.94