2018

How to find common variants in multiple VCF files 2018/07/25

dDocent install successes & failures on Linux supercomputers 2018/03/10

2017

How To Setup A Linux Supercomputer for RAD-seq 2017/09/17

Analyzing ddRADseq Data in SNAPP 2017/09/13

Running AMOVA (analysis of molecular variance) on biallelic SNP data in R 2017/08/18

2013

Where to outsource next-generation sequencing runs for de novo SNP discovery for phylogenetics and phylogeography 2013/11/27