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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 PICO Portal from OpenAlex.

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

PICO Portalcitation count

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

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

PICO Portalyear

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

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

PICO Portaloa status

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

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

PICO Portaldoi

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?

PICO Portalpmid

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?

PICO Portalopenalex

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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