Back to search

Article

Long read nanopore sequencing for detection of HLA and CYP2D6 variants and haplotypes

2015-01-21

Abstract excerpt

<ns4:p> Haplotypes are often critical for the interpretation of genetic laboratory observations into medically actionable findings. Current massively parallel DNA sequencing technologies produce short sequence reads that are often unable to resolve haplotype information. Phasing short read data typically requires supplemental statistical phasing based on known haplotype structure in the population or parental geno...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
580d1e96-e31d-59e3-a133-70840a6574c7
DOI
10.12688/f1000research.6037.1
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Long read nanopore sequencing for detection of HLA and CYP2D6 variants and haplotypesDOI 10.12688/f1000research.6037.1
Select a neighboring publication to make it the new centre.