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BACOM: in silico detection of genomic deletion types and correction of normal cell contamination in copy number data.
Bioinformatics. 2011 Jun 1;27(11):1473-80. doi: 10.1093/bioinformatics/btr183. Epub 2011 Apr 15.
2
Genome-wide identification of significant aberrations in cancer genome.
BMC Genomics. 2012 Jul 27;13:342. doi: 10.1186/1471-2164-13-342.
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AISAIC: a software suite for accurate identification of significant aberrations in cancers.
Bioinformatics. 2014 Feb 1;30(3):431-3. doi: 10.1093/bioinformatics/btt693. Epub 2013 Nov 29.
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VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing.
Genome Res. 2012 Mar;22(3):568-76. doi: 10.1101/gr.129684.111. Epub 2012 Feb 2.
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TAGCNA: a method to identify significant consensus events of copy number alterations in cancer.
PLoS One. 2012;7(7):e41082. doi: 10.1371/journal.pone.0041082. Epub 2012 Jul 18.
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Hierarchical discovery of large-scale and focal copy number alterations in low-coverage cancer genomes.
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Minimum error calibration and normalization for genomic copy number analysis.
Genomics. 2020 Sep;112(5):3331-3341. doi: 10.1016/j.ygeno.2020.05.008. Epub 2020 May 13.

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Obtaining spatially resolved tumor purity maps using deep multiple instance learning in a pan-cancer study.
Patterns (N Y). 2021 Dec 9;3(2):100399. doi: 10.1016/j.patter.2021.100399. eCollection 2022 Feb 11.
2
MFCNV: A New Method to Detect Copy Number Variations From Next-Generation Sequencing Data.
Front Genet. 2020 May 15;11:434. doi: 10.3389/fgene.2020.00434. eCollection 2020.
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Accurate Inference of Tumor Purity and Absolute Copy Numbers From High-Throughput Sequencing Data.
Front Genet. 2020 Apr 30;11:458. doi: 10.3389/fgene.2020.00458. eCollection 2020.
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DBS: a fast and informative segmentation algorithm for DNA copy number analysis.
BMC Bioinformatics. 2019 Jan 3;20(1):1. doi: 10.1186/s12859-018-2565-8.
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Integrated Proteogenomic Characterization of Human High-Grade Serous Ovarian Cancer.
Cell. 2016 Jul 28;166(3):755-765. doi: 10.1016/j.cell.2016.05.069. Epub 2016 Jun 29.
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Integration of Network Biology and Imaging to Study Cancer Phenotypes and Responses.
IEEE/ACM Trans Comput Biol Bioinform. 2014 Nov-Dec;11(6):1009-19. doi: 10.1109/TCBB.2014.2338304. Epub 2014 Jul 16.
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UNDO: a Bioconductor R package for unsupervised deconvolution of mixed gene expressions in tumor samples.
Bioinformatics. 2015 Jan 1;31(1):137-9. doi: 10.1093/bioinformatics/btu607. Epub 2014 Sep 10.
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AbsCN-seq: a statistical method to estimate tumor purity, ploidy and absolute copy numbers from next-generation sequencing data.
Bioinformatics. 2014 Apr 15;30(8):1056-1063. doi: 10.1093/bioinformatics/btt759. Epub 2014 Jan 2.

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2
Copy number analysis indicates monoclonal origin of lethal metastatic prostate cancer.
Nat Med. 2009 May;15(5):559-65. doi: 10.1038/nm.1944. Epub 2009 Apr 12.
4
Estimation and assessment of raw copy numbers at the single locus level.
Bioinformatics. 2008 Mar 15;24(6):759-67. doi: 10.1093/bioinformatics/btn016. Epub 2008 Jan 19.
6
Assessing the significance of chromosomal aberrations in cancer: methodology and application to glioma.
Proc Natl Acad Sci U S A. 2007 Dec 11;104(50):20007-12. doi: 10.1073/pnas.0710052104. Epub 2007 Dec 6.
8
SiDCoN: a tool to aid scoring of DNA copy number changes in SNP chip data.
PLoS One. 2007 Oct 31;2(10):e1093. doi: 10.1371/journal.pone.0001093.
10
High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping.
Genome Res. 2006 Sep;16(9):1136-48. doi: 10.1101/gr.5402306. Epub 2006 Aug 9.

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