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Tools for Data Science in Genomic Sequencing.

This repository includes projects using Python, R Language, Bioconductor, and Galaxy to understand, analyze, and interpret data from next-generation sequencing experiments.

The following projects are included:

Set up a workflow to analyse DNA polymorphic sites of father-mother-child sequencing samples

This project includes a set of tools for DNA sequence analysis (

a. check records in file (count_records), b. compute the length of each DNA sequence (check_length), c. identify open read frame in each DNA sequence (orf_identifier), d. identify repeated motif in sequence (repeats_identifier) ).

This project apply bowtie2, samtools, bedtools and bcftools to:

  1. Analyze RNA-seq data to determine sets of genes that are expressed in the various tissues;
  2. cataloging genetic variation using SAMtools and BEDtools as well as other Unix commands;
  3. develop a pipeline for variant calling in a given genome; 4) perform the bioinformatics analysis to determine genes that are differentially expressed at different experimental conditions with Linux command line.

Python is used to implement key algorithms and data structures to analyze real genomes and DNA sequencing datasets.

Use tools from the Bioconductor project and R programming language to analyze genomic data.

An introduction to the statistics for analysis of genomic data.

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projects using galaxy, python, linux command line to analyze sequencing data

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  • Python 46.6%
  • R 28.7%
  • Rich Text Format 24.7%