tsy19900929 / snpeffToMaf
Converts snpeff annotations into MAF
☆11Updated 8 months ago
Alternatives and similar repositories for snpeffToMaf
Users that are interested in snpeffToMaf are comparing it to the libraries listed below
Sorting:
- ☆53Updated 2 years ago
- SMN1 copy-number and sequence variant analysis from next generation sequencing data☆22Updated 2 years ago
- ☆39Updated last year
- SpecHLA reconstructs entire diploid sequences of HLA genes and infers LOH events. It supports HLA-A, -B, -C, -DPA1, -DPB1, -DQA1, -DQB1, …☆43Updated last month
- Public Benchmark of Long-Read Structural Variant Caller on PacBio CCS HG002 Data☆50Updated 4 years ago
- Tools for processing and analyzing structural variants.☆33Updated 9 years ago
- Robust detection of clinically relevant structural and copy number variation from whole genome sequencing data☆69Updated 8 months ago
- CN-Learn☆29Updated 5 years ago
- ClassifyCNV: a tool for clinical annotation of copy-number variants