Computational analysis of RNA-seq.
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[1] R. O’Neill,et al. Abundant Human DNA Contamination Identified in Non-Primate Genome Databases , 2011, PloS one.
[2] Paul D. Shaw,et al. BIOINFORMATICS APPLICATIONS NOTE , 2022 .
[3] Gonçalo R. Abecasis,et al. The Sequence Alignment/Map format and SAMtools , 2009, Bioinform..
[4] Jonathan A. Eisen,et al. BioTorrents: A File Sharing Service for Scientific Data , 2010, PloS one.
[5] S. Lewis,et al. The generic genome browser: a building block for a model organism system database. , 2002, Genome research.
[6] Dennis B. Troup,et al. NCBI GEO: archive for functional genomics data sets—10 years on , 2010, Nucleic Acids Res..
[7] Ibrahim Emam,et al. ArrayExpress update—an archive of microarray and high-throughput sequencing-based functional genomics experiments , 2010, Nucleic Acids Res..
[8] Cole Trapnell,et al. Ultrafast and memory-efficient alignment of short DNA sequences to the human genome , 2009, Genome Biology.
[9] Dawn H. Nagel,et al. The B73 Maize Genome: Complexity, Diversity, and Dynamics , 2009, Science.
[10] Nansheng Chen,et al. Using RepeatMasker to Identify Repetitive Elements in Genomic Sequences , 2009, Current protocols in bioinformatics.
[11] Lior Pachter,et al. Sequence Analysis , 2020, Definitions.
[12] P Green,et al. Base-calling of automated sequencer traces using phred. II. Error probabilities. , 1998, Genome research.
[13] C. Vicient. Transcriptional activity of transposable elements in maize , 2010, BMC Genomics.
[14] B. Dujon,et al. Comparative Genomics and Molecular Dynamics of DNA Repeats in Eukaryotes , 2008, Microbiology and Molecular Biology Reviews.
[15] Cole Trapnell,et al. Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation. , 2010, Nature biotechnology.
[16] P. Green,et al. Base-calling of automated sequencer traces using phred. I. Accuracy assessment. , 1998, Genome research.