User:Konrad U Foerstner/Tools and procedures: Difference between revisions

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* [https://github.com/pymc-devs/pymc PyMC] - Bayesian inference in Python
* [https://github.com/pymc-devs/pymc PyMC] - Bayesian inference in Python
* [https://pypi.python.org/pypi/matplotlib-venn matplotlib-venn] - Venn diagrams in matplotlib
* [https://pypi.python.org/pypi/matplotlib-venn matplotlib-venn] - Venn diagrams in matplotlib
* [https://github.com/daler/gffutils gffutils]


=== Misc ===
=== Misc ===

Revision as of 04:54, 9 September 2013

SNP calling

With Samtools


Phylogenetic trees

Multiple alignments

TSS prediction

Whole genome alignments

Pathway visualization

Transcription Terminator prediction

miRNA target prediction

miRmap (untested)

Differential gene expression analysis

DESeq

  • Tips:
    • small count noise - sequence deeper
    • large count noise - sequence more replicates
    • if the assumption that most genes are not differentially expressed is not the case use different methods to normalize (e.g. spike-ins)

Others

  • BaySEq
  • edgR
  • Gfold
  • NoiSeq

Python

General useful libraries

Misc


Visualisation