Comprehensive benchmarking of somatic single-nucleotide variant and indel detection at ultra-low allele fractions using short- and long-read data
利用短读长和长读长数据对超低等位基因频率下的体细胞单核苷酸变异和插入缺失检测进行全面基准测试
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影响因子:
doi:10.1101/2025.10.13.681545
Jiny Ha, Yoo-Jin; Maziec, Dominika; Markowski, Julia; Georges, Stephanie J; Parmalee, Nancy L; Berselli, Michele; Coorens, Tim H H; Dong, Shihua; Gardiner, Stephanie; Kalra, Divya; Li, Daofeng; Miao, Benpeng; Musunuri, Rajeeva; Xue, Liying; Yu, Zhi; Walker, Kimberly; Anderson, Lisa; Au, Natalie Y T; Cibulskis, Carrie; Doddapaneni, Harsha; Grochowski, Christopher M; Jensen, Dana M; Lindsay, Tina; Loy, Kelsey; Narayan, Azeet; Narzisi, Giuseppe; Ou, Jeffrey; Pham, Meranda M; Runnels, Alexi M; Stergachis, Andrew B; Sutherlin, Lila M; Wang, Ting; Jin, Hu; Feng, William C; Zhang, Yuwei; Veit, Alexander D; TaeHee Kim, Clara; Chun, Hye-Jung E; Ardlie, Kristin; Fulton, Robert S; Germer, Soren; Gibbs, Richard; Marth, Gabor T; Bennett, James T; Park, Peter J
