Developing an Integrated Genomic Profile for Cancer Patients with the Use of NGS Data
暂无分享,去创建一个
[1] David G Hendrickson,et al. Differential analysis of gene regulation at transcript resolution with RNA-seq , 2012, Nature Biotechnology.
[2] Dimitrios Zafeiris,et al. An Artificial Neural Network Integrated Pipeline for Biomarker Discovery Using Alzheimer's Disease as a Case Study , 2018, Computational and structural biotechnology journal.
[3] Christos G. Cassandras,et al. Integrating mutation and gene expression cross-sectional data to infer cancer progression , 2016, BMC Systems Biology.
[4] Emili Montserrat,et al. Genetic lesions in chronic lymphocytic leukemia: what’s ready for prime time use? , 2010, Haematologica.
[5] Gaël Varoquaux,et al. Scikit-learn: Machine Learning in Python , 2011, J. Mach. Learn. Res..
[6] Bo Li,et al. VIPER: Visualization Pipeline for RNA-seq, a Snakemake workflow for efficient and complete RNA-seq analysis , 2018, BMC Bioinformatics.
[7] Héctor Corrada Bravo,et al. Epiviz: interactive visual analytics for functional genomics data , 2014, Nature Methods.
[8] Giovanni Felici,et al. Combining DNA methylation and RNA sequencing data of cancer for supervised knowledge extraction , 2018, BioData Mining.
[9] Cole Trapnell,et al. Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation. , 2010, Nature biotechnology.
[10] Mattia D'Antonio,et al. WEP: a high-performance analysis pipeline for whole-exome data , 2013, BMC Bioinformatics.
[11] Yan Guo,et al. Architectures and accuracy of artificial neural network for disease classification from omics data , 2019, BMC Genomics.
[12] H. Hakonarson,et al. ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data , 2010, Nucleic acids research.
[13] Lior Pachter,et al. Sequence Analysis , 2020, Definitions.
[14] Helga Thorvaldsdóttir,et al. Integrative Genomics Viewer , 2011, Nature Biotechnology.
[15] D. Hume,et al. Exome Sequencing: Current and Future Perspectives , 2015, G3: Genes, Genomes, Genetics.
[16] M. Nagymihály,et al. Next-Generation Sequencing and its new possibilities in medicine , 2015 .
[17] Christopher Gignoux,et al. The 1000 Genomes Project: new opportunities for research and social challenges , 2010, Genome Medicine.
[18] B. Gener,et al. Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders , 2015, Molecular Autism.
[19] Shuying Sun,et al. Integrative analysis of gene expression and methylation data for breast cancer cell lines , 2018, BioData Mining.
[20] B. Dörken,et al. EGR2 mutations define a new clinically aggressive subgroup of chronic lymphocytic leukemia , 2017, Leukemia.
[21] Jeffrey T Leek,et al. Transcript-level expression analysis of RNA-seq experiments with HISAT, StringTie and Ballgown , 2016, Nature Protocols.
[22] M. Gerstein,et al. RNA-Seq: a revolutionary tool for transcriptomics , 2009, Nature Reviews Genetics.
[23] Scott D. Kahn. On the Future of Genomic Data , 2011, Science.
[24] E. Boerwinkle,et al. dbNSFP: A Lightweight Database of Human Nonsynonymous SNPs and Their Functional Predictions , 2011, Human mutation.
[25] David R. Kelley,et al. Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks , 2012, Nature Protocols.
[26] Kai Wang,et al. SeqMule: automated pipeline for analysis of human exome/genome sequencing data , 2015, Scientific Reports.
[27] Christopher R. Cabanski,et al. Integrated RNA and DNA sequencing improves mutation detection in low purity tumors , 2014, Nucleic acids research.
[28] Subhajyoti De,et al. IMPACT: a whole-exome sequencing analysis pipeline for integrating molecular profiles with actionable therapeutics in clinical samples , 2016, J. Am. Medical Informatics Assoc..
[29] Nuno A. Fonseca,et al. iRAP - an integrated RNA-seq Analysis Pipeline , 2014, bioRxiv.
[30] Bruno Zeitouni,et al. Abstract 2701: Combining whole-exome and RNA-Seq data improves the quality of PDX mutation profiles , 2016 .
[31] Steven R. Head,et al. Next-generation sequencing , 2010, Nature Reviews Drug Discovery.