haplotype variant
Evidence from:
primary |
all sources
No related entities found.
Mentioned in (6)
Papers in which this entity is mentioned.
- Parent-of-origin effects on complex traits in up to 236,781 individuals. (2025)
- Nanopore sequencing with unique molecular identifiers enables accurate mutation analysis and haplotyping in the complex lipoprotein(a) KIV-2 VNTR. (2024)
- Integrative reconstruction of cancer genome karyotypes using InfoGenomeR. (2021)
- ASEP: Gene-based detection of allele-specific expression across individuals in a population by RNA sequencing. (2020)
- Genome-wide somatic variant calling using localized colored de Bruijn graphs. (2018)
- Immune diversity sheds light on missing variation in worldwide genetic diversity panels. (2018)
Merged raw entities (4)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| haplotype | variant | 18 | 21 |
| composite genomic element | variant | — | — |
| gg haplotype | variant | — | — |
| haplotype pair | variant | — | — |