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Proteomics_Customized-Tool-to-visualize-protein-coverage-after-Maxquant-search-for-MS-data
Proteomics_Customized-Tool-to-visualize-protein-coverage-after-Maxquant-search-for-MS-data PublicTool to show protein coverage across different samples/condition, using the Maxquant output file "peptdies.txt"
R 2
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RNAseq_Non-template-additions-to-the-sequencing-reads
RNAseq_Non-template-additions-to-the-sequencing-reads Publicdetect and count non template additions to the sequencing reads, useful for polyA detection and other modification to RNA
Perl 1
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General_Loop-through-files
General_Loop-through-files PublicLoop through files and do something
Shell
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RNAseq_Mapping-the-Number-of-differences-per-Chromosome-in-RNA-seq-alignment-sam-file
RNAseq_Mapping-the-Number-of-differences-per-Chromosome-in-RNA-seq-alignment-sam-file PublicMapping the Number of differences (Mismatch/deletion/Insertion) per Chromosome/strand in RNA-seq alignment sam file
Perl
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RNAseq_SAM_file_flag_summary
RNAseq_SAM_file_flag_summary Publicperl script to summarize flag values and thier counts in SAMfile
Perl
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