A universal SNP and small-indel variant caller using deep neural networks.
Nat Biotechnol. 2018 Nov;36(10):983-987. doi: 10.1038/nbt.4235. Epub 2018 Sep 24.
Nat Biotechnol. 2018.
PMID: 30247488
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| Year | Number of Results |
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On the identifiability of the isoform deconvolution problem: application to select the proper fragment length in an RNA-seq library.
Bioinformatics. 2022 Mar 4;38(6):1491-1496. doi: 10.1093/bioinformatics/btab873.
Bioinformatics. 2022.
PMID: 34978563
Free PMC article.
Gaining comprehensive biological insight into the transcriptome by performing a broad-spectrum RNA-seq analysis.
Nat Commun. 2017 Jul 5;8(1):59. doi: 10.1038/s41467-017-00050-4.
Nat Commun. 2017.
PMID: 28680106
Free PMC article.
COSINE: non-seeding method for mapping long noisy sequences.
Nucleic Acids Res. 2017 Aug 21;45(14):e132. doi: 10.1093/nar/gkx511.
Nucleic Acids Res. 2017.
PMID: 28586438
Free PMC article.
Characterization of the human ESC transcriptome by hybrid sequencing.
Proc Natl Acad Sci U S A. 2013 Dec 10;110(50):E4821-30. doi: 10.1073/pnas.1320101110. Epub 2013 Nov 26.
Proc Natl Acad Sci U S A. 2013.
PMID: 24282307
Free PMC article.
An ensemble approach to accurately detect somatic mutations using SomaticSeq.
Genome Biol. 2015 Sep 17;16(1):197. doi: 10.1186/s13059-015-0758-2.
Genome Biol. 2015.
PMID: 26381235
Free PMC article.
Characterization of fusion genes and the significantly expressed fusion isoforms in breast cancer by hybrid sequencing.
Nucleic Acids Res. 2015 Oct 15;43(18):e116. doi: 10.1093/nar/gkv562. Epub 2015 Jun 3.
Nucleic Acids Res. 2015.
PMID: 26040699
Free PMC article.
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