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Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence

PaperCitations, authors & open-access status

Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence is a paper indexed in ScholarIQ from OpenAlex.

How many citations does Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence have?

ScholarIQcitation count

Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence has 261 citations in the OpenAlex counts ScholarIQ stores.

When was Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence published?

ScholarIQyear

Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence has 2003 year in the ScholarIQ index.

What is the open-access status of Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence?

ScholarIQoa status

Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence has gold oa status in the ScholarIQ index.

What is the DOI of Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence?

ScholarIQdoi

The DOI for Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence is on the source record.

What is the PMID of Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence?

ScholarIQpmid

The PMID for Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence is on the source record.

What is the OpenAlex record for Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence?

ScholarIQopenalex

The OpenAlex for Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence is on the source record.

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