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1. 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 Public

   Tool to show protein coverage across different samples/condition, using the Maxquant output file "peptdies.txt"

   R 2

2. RNAseq_Non-template-additions-to-the-sequencing-reads RNAseq_Non-template-additions-to-the-sequencing-reads Public

   detect and count non template additions to the sequencing reads, useful for polyA detection and other modification to RNA

   Perl 1

3. General_Loop-through-files General_Loop-through-files Public

   Loop through files and do something

   Shell

4. 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 Public

   Mapping the Number of differences (Mismatch/deletion/Insertion) per Chromosome/strand in RNA-seq alignment sam file

   Perl

5. RNAseq_SAM_file_flag_summary RNAseq_SAM_file_flag_summary Public

   perl script to summarize flag values and thier counts in SAMfile

   Perl