User:Herrer01: Difference between revisions

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(Created page with "== Juan Manuel Herrero Medrano == Postdoctoral position at Wageningen University, Animal Breeding and Genomics Centre. '''Scientific interests:''' * Bioinformatics * Next...")
 
 
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'''Main current projects'''
'''Main current projects'''
* Storage, mapping variants calling analysis on re-sequence data on various livestock species
* Storage, mapping variants calling analysis on re-sequence data on various livestock species
* Functional aspects of genome variation in Turkey
* Functional aspects of turkey genome variation
* De novo assembly and annotation of genomes
* De novo assembly and annotation of genomes


'''Procedures'''
'''Procedures'''
* Main sequencing platform is Illumina (We started in 2008 on Solexa GA, to currently Illumina HiSeq).
* Main sequencing platform is Illumina (We started in 2008 on Solexa GA, to currently Illumina HiSeq).
* Depending on research questions various short-read mapping programs are used (Mosaik, BWA, BWA/Stampy, MrsFAST)
* Short-read mapping (Mosaik, BWA)
* Variant calling (Samtools, GATK).
* Variant calling (Samtools, GATK, ANGSD).
* Functional analysis of variants (Annovar, Variant Effect Predictor)
* Functional analysis of variants (Annovar, Variant Effect Predictor)
* Various population- and phylogenomic approaches  
* Various population- and phylogenomic approaches  

Latest revision as of 11:16, 19 February 2015

Juan Manuel Herrero Medrano

Postdoctoral position at Wageningen University, Animal Breeding and Genomics Centre.

Scientific interests:

  • Bioinformatics
  • Next Generation Sequence data and High-density SNP arrays analysis
  • Functional genomics
  • Population genomics

Main current projects

  • Storage, mapping variants calling analysis on re-sequence data on various livestock species
  • Functional aspects of turkey genome variation
  • De novo assembly and annotation of genomes

Procedures

  • Main sequencing platform is Illumina (We started in 2008 on Solexa GA, to currently Illumina HiSeq).
  • Short-read mapping (Mosaik, BWA)
  • Variant calling (Samtools, GATK, ANGSD).
  • Functional analysis of variants (Annovar, Variant Effect Predictor)
  • Various population- and phylogenomic approaches

Main programming languages:

  • Linux shell scripting
  • Python
  • R