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Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel

PaperCitations, authors & open-access status

Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel is a paper indexed in ScholarIQ from OpenAlex.

How many citations does Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel have?

ScholarIQcitation count

Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel has 460 citations in the OpenAlex counts ScholarIQ stores.

When was Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel published?

ScholarIQyear

Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel has 2014 year in the ScholarIQ index.

What is the open-access status of Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel?

ScholarIQoa status

Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel has bronze oa status in the ScholarIQ index.

What is the DOI of Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel?

ScholarIQdoi

The DOI for Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel is on the source record.

What is the PMID of Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel?

ScholarIQpmid

The PMID for Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel is on the source record.

What is the OpenAlex record for Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel?

ScholarIQopenalex

The OpenAlex for Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel is on the source record.

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