reference allele variant
Evidence from:
primary |
all sources
No related entities found.
Mentioned in (9)
Papers in which this entity is mentioned.
- Discovery of regulatory noncoding variants in individual cancer genomes by using cis-X. (2020)
- Ploidy- and Purity-Adjusted Allele-Specific DNA Analysis Using CLONETv2. (2019)
- PASSPORT-seq: A Novel High-Throughput Bioassay to Functionally Test Polymorphisms in Micro-RNA Target Sites. (2018)
- Mapping and phasing of structural variation in patient genomes using nanopore sequencing. (2017)
- Eigenanalysis of SNP data with an identity by descent interpretation. (2016)
- GeneiASE: Detection of condition-dependent and static allele-specific expression from RNA-seq data without haplotype information. (2016)
- MBASED: allele-specific expression detection in cancer tissues and cell lines. (2014)
- VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing. (2012)
- Nucleotide-resolution analysis of structural variants using BreakSeq and a breakpoint library. (2010)
Merged raw entities (2)
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 |
|---|---|---|---|
| reference allele | variant | 12 | 12 |
| r | variant | 1 | 1 |