zzwch / myScripts

some scripts to be used again

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myScripts

circleInteractionBetween2CellType R function
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gradient_2d.R image

single cell RNA-Seq analysis method

pcurve princurve:principal curves
ggrepel: Repel overlapping text labels away from each other. https://github.com/slowkow/ggrepel  
RSeQC: An RNA-seq Quality Control Package http://rseqc.sourceforge.net

useful tools

Command Line Interface Creation Kit [:thumbsup:] Python composable command line utility http://click.pocoo.org/
bam2fastx only converts the unmapped reads from the input file, discarding those unmapped reads flagged as QC failed.
bedtools: a powerful toolset for genome arithmetic http://bedtools.readthedocs.io http://www.cureffi.org/2013/11/18/an-mrna-seq-pipeline-using-gsnap-samtools-cufflinks-and-bedtools/
deepTools: tools for exploring deep sequencing data https://deeptools.readthedocs.io/en/develop/

Waddinton Epigenetic Landscape

Waddington Plot using ggplot2 R package image

BioSoft

  • CrossMap
    • CrossMap is a program for convenient conversion of genome coordinates (or annotation files) between different assemblies (such as Human hg18 (NCBI36) <> hg19 (GRCh37), Mouse mm9 (MGSCv37) <> mm10 (GRCm38)).
    • It supports most commonly used file formats including SAM/BAM, Wiggle/BigWig, BED, GFF/GTF, VCF.
    • CrossMap is designed to liftover genome coordinates between assemblies. It’s not a program for aligning sequences to reference genome.
    • http://crossmap.sourceforge.net/#convert-gff-gtf-format-files

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some scripts to be used again


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