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Family-Based Haplotype Estimation and Allele Dosage Correction for Polyploids Using Short Sequence Reads
DNA sequence reads contain information about the genomic variants located on a single chromosome. By extracting and extending this information using the overlaps between the reads, the haplotypes of an individual can be obtained. Using parent-offspring relationships in a population can considerably...
Tallennettuna:
| Julkaisussa: | Front Genet |
|---|---|
| Päätekijät: | , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Frontiers Media S.A.
2019
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6477055/ https://ncbi.nlm.nih.gov/pubmed/31040862 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2019.00335 |
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