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Accession: PRJNA677997 ID: 677997

Homo sapiens (human)

SEQC2 Onco-panel Sequencing Working Group - PanCancer panel Study

See Genome Information for Homo sapiens
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82763 additional projects are related by organism.
PanCancer panel study with the validated genomic reference material
AccessionPRJNA677997
Data TypeRaw sequence reads, Variation
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
PublicationsGong B et al., "Cross-oncopanel study reveals high sensitivity and accuracy with overall analytical performance depending on genomic regions.", Genome Biol, 2021 Apr 16;22(1):109
Grants
  • "Comprehensive Assessments of Deep Targeted Sequencing for Detecting Rare Subclonal Mutations" (Grant ID E0767001, US Food and Drug Administration)
SubmissionRegistration date: 12-Nov-2020
SEquence Quality Control consortium
- National Center for Toxicological Research
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments503
Publications
PubMed1
PMC1
Other datasets
BioSample5
SRA Data Details
ParameterValue
Data volume, Gbases16,425
Data volume, Tbytes5.84

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    SEQC2 Onco-panel Sequencing Working Group - PanCancer panel Study
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