Similarities and differences between variants called with human reference genome HG19 or HG38.
Pan, Bohu; Kusko, Rebecca; Xiao, Wenming; Zheng, Yuanting; Liu, Zhichao; Xiao, Chunlin; Sakkiah, Sugunadevi; Guo, Wenjing; Gong, Ping; Zhang, Chaoyang; Ge, Weigong; Shi, Leming; Tong, Weida; Hong, Huixiao.
; 20(Suppl 2): 101, 2019 Mar 14.
Artigo em Inglês | MEDLINE | ID: mdl-30871461
The role of replicates for error mitigation in next-generation sequencing.
Advancements in Next-Generation Sequencing.
Detection of runs of homozygosity from whole exome sequencing data: state of the art and perspectives for clinical, population and epidemiological studies.
What are people willing to pay for whole-genome sequencing information, and who decides what they receive?
Anchored pseudo-de novo assembly of human genomes identifies extensive sequence variation from unmapped sequence reads.
High-Accuracy HLA Type Inference from Whole-Genome Sequencing Data Using Population Reference Graphs.
A reference data set of 5.4 million phased human variants validated by genetic inheritance from sequencing a three-generation 17-member pedigree.
Mining Metagenomic Data Sets for Ancient DNA: Recommended Protocols for Authentication.
Genome-wide footprinting: ready for prime time?
Sequencing pools of individuals - mining genome-wide polymorphism data without big funding.