Using ERDS to infer copy-number variants in high-coverage genomes.

No abstract is available for this paper.

• Publication year

  2012

• Venue

  American Journal of Human Genetics

• Publication date

  2012-09-07

• Fields of study

  Biology, Medicine, Computer Science

• Identifiers
  DOI 10.1016/j.ajhg.2012.07.004PMID 22939633PMCID PMC3511991
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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