KATK: Fast genotyping of rare variants directly from unmapped sequencing reads
Author:
Affiliation:
1. Department of Bioinformatics, Institute of Molecular and Cell Biology University of Tartu Tartu Estonia
Funder
European Regional Development Fund
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.24197
Reference46 articles.
1. A global reference for human genetic variation
2. Mapping-free variant calling using haplotype reconstruction from k-mer frequencies
3. The emerging clinical relevance of genomics in cancer medicine
4. Rapid Genome Sequencing in the Critically Ill
5. Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohorts
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. GeneToCN: an alignment-free method for gene copy number estimation directly from next-generation sequencing reads;Scientific Reports;2023-10-18
2. GeneToCN: an alignment-free method for gene copy number estimation directly from next-generation sequencing reads;2023-06-04
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