Title | Scopus | WOS | PubMed | Scopus | WOS | PubMed | Scopus | WOS | PubMed | |
---|---|---|---|---|---|---|---|---|---|---|
A multi-task convolutional deep neural network for variant calling in single molecule sequencing Journal:Nature Communications | ||||||||||
Assembly-free discovery of human novel sequences using long reads. Journal:DNA Research | ||||||||||
BASE: a practical de novo assembler for large genomes using long NGS reads Journal:BMC Genomics | ||||||||||
Boosting variant-calling performance with multi-platform sequencing data using Clair3-MP Journal:BMC Bioinformatics | ||||||||||
Building a Chinese pan-genome of 486 individuals Journal:Communications Biology | ||||||||||
Compressed indexing and local alignment of DNA Journal:Bioinformatics | ||||||||||
database.bio: A web application for interpreting human variations Journal:Bioinformatics |
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