Wang K - Search Results

1

Phen2Gene: rapid phenotype-driven gene prioritization for rare diseases.

Zhao M, Havrilla JM, Fang L, Chen Y, Peng J, Liu C, Wu C, Sarmady M, Botas P, Isla J, Lyon GJ, Weng C, Wang K. Zhao M, et al. Among authors: wang k. NAR Genom Bioinform. 2020 Jun;2(2):lqaa032. doi: 10.1093/nargab/lqaa032. Epub 2020 May 25. NAR Genom Bioinform. 2020. PMID: 32500119 Free PMC article.

2

PhenCards: a data resource linking human phenotype information to biomedical knowledge.

Havrilla JM, Liu C, Dong X, Weng C, Wang K. Havrilla JM, et al. Among authors: wang k. Genome Med. 2021 May 25;13(1):91. doi: 10.1186/s13073-021-00909-8. Genome Med. 2021. PMID: 34034817 Free PMC article.

3

NextSV: a meta-caller for structural variants from low-coverage long-read sequencing data.

Fang L, Hu J, Wang D, Wang K. Fang L, et al. Among authors: wang k, wang d. BMC Bioinformatics. 2018 May 23;19(1):180. doi: 10.1186/s12859-018-2207-1. BMC Bioinformatics. 2018. PMID: 29792160 Free PMC article.

4

Polishing high-quality genome assemblies.

Fang L, Wang K. Fang L, et al. Among authors: wang k. Nat Methods. 2022 Jun;19(6):649-650. doi: 10.1038/s41592-022-01515-1. Nat Methods. 2022. PMID: 35610477 No abstract available.

5

Identification of Copy Number Variants from SNP Arrays Using PennCNV.

Fang L, Wang K. Fang L, et al. Among authors: wang k. Methods Mol Biol. 2018;1833:1-28. doi: 10.1007/978-1-4939-8666-8_1. Methods Mol Biol. 2018. PMID: 30039360

6

LongGF: computational algorithm and software tool for fast and accurate detection of gene fusions by long-read transcriptome sequencing.

Liu Q, Hu Y, Stucky A, Fang L, Zhong JF, Wang K. Liu Q, et al. Among authors: wang k. BMC Genomics. 2020 Dec 29;21(Suppl 11):793. doi: 10.1186/s12864-020-07207-4. BMC Genomics. 2020. PMID: 33372596 Free PMC article.

7

Expediting knowledge acquisition by a web framework for Knowledge Graph Exploration and Visualization (KGEV): case studies on COVID-19 and Human Phenotype Ontology.

Peng J, Xu D, Lee R, Xu S, Zhou Y, Wang K. Peng J, et al. Among authors: wang k. BMC Med Inform Decis Mak. 2022 Jun 2;22(Suppl 2):147. doi: 10.1186/s12911-022-01848-z. BMC Med Inform Decis Mak. 2022. PMID: 35655307 Free PMC article.

8

NanoCaller for accurate detection of SNPs and indels in difficult-to-map regions from long-read sequencing by haplotype-aware deep neural networks.

Ahsan MU, Liu Q, Fang L, Wang K. Ahsan MU, et al. Among authors: wang k. Genome Biol. 2021 Sep 6;22(1):261. doi: 10.1186/s13059-021-02472-2. Genome Biol. 2021. PMID: 34488830 Free PMC article.

9

LIQA: long-read isoform quantification and analysis.

Hu Y, Fang L, Chen X, Zhong JF, Li M, Wang K. Hu Y, et al. Among authors: wang k. Genome Biol. 2021 Jun 17;22(1):182. doi: 10.1186/s13059-021-02399-8. Genome Biol. 2021. PMID: 34140043 Free PMC article.

10

LinkedSV for detection of mosaic structural variants from linked-read exome and genome sequencing data.

Fang L, Kao C, Gonzalez MV, Mafra FA, Pellegrino da Silva R, Li M, Wenzel SS, Wimmer K, Hakonarson H, Wang K. Fang L, et al. Among authors: wang k. Nat Commun. 2019 Dec 6;10(1):5585. doi: 10.1038/s41467-019-13397-7. Nat Commun. 2019. PMID: 31811119 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

40,234 results

Search Page

Filters