Thank you for your interest. Here, in the Institute of Veterinary Genetics in Argentina, we are using BioSmalltalk since a few years. Most of my workflows are related with population genetics and phylogeography. Specifically I've used BioSmalltalk recently to interface PLINK 1.9, to generate input files and plot output for LAMP-LD (local ancestry inference), to run ShapeIt and PHASE (haplotype inference), generate code for rehh (detection of footprints of selection) and PhyloclassTalk for determining haplogroups using mtDNA geo-annotated sequences. NGS is a domain which I started to work actively since one year ago, but more applied to RNASeq than WGS. Right now, I am designing an object model to compare outputs from several trimmers, aligners and gene expression packages.
I would recommend BioSmalltalk to anyone who want more than copy and paste of bioinformatics snippets or commands. Definitely it is the ideal choice for someone who already knows Smalltalk and is learning sequence analysis, or want to model complex domains which are not very well explored or researched. Although other Bio* libraries currently seem to have more classes, too often is *very* difficult to evolve their code, i.e. to change something to do more than the documented examples.
Currently, I am trying to get an installer with more features, but in the meantime to install latest developement of BioSmalltalk, just open Pharo 5 and evaluate (tested on Windows 8.1):
Metacello new
smalltalkhubUser: 'hernan' project: 'BioSmalltalk';
configuration: 'BioSmalltalk';
version: #bleedingEdge;
load
Let me know if you have specific requirements or analysis in mind.
Best regards,
Hernán