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A reference haplotype panel for genome-wide imputation of short tandem repeats
Short tandem repeats (STRs) are involved in dozens of Mendelian disorders and have been implicated in complex traits. However, genotyping arrays used in genome-wide association studies focus on single nucleotide polymorphisms (SNPs) and do not readily allow identification of STR associations. We lev...
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| Foilsithe in: | Nat Commun |
|---|---|
| Main Authors: | , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Nature Publishing Group UK
2018
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6199332/ https://ncbi.nlm.nih.gov/pubmed/30353011 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41467-018-06694-0 |
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