The Variant Effect Predictor predicts the functional effects of genomic variants
We have implemented a tool called VSEARCH which supports de novo and reference based chimera detection, clustering, full-length and prefix dereplication, reverse complementation, masking, all-vs-all pairwise global alignment, exact and global alignment searching, shuffling, subsampling and sorting. It also supports FASTQ file analysis, filtering and conversion.
a variant tool set that discovers short variants from Next Generation Sequencing data
WebLogo is a web based application designed to make the generation of sequence logos as easy and painless as possible.
Celera Assembler is a de novo whole-genome shotgun (WGS) DNA sequence assembler.
The wigToBigWig program converts a ‘wig’ file to ‘bigWig’ format.
Wise2 includes genewise, a program for aligning proteins or protein HMMs to DNA, and dynamite a rather cranky “macro language”” which automates the production of dynamic programming. “
TopHat is a program that aligns RNA-Seq reads to a genome in order to identify exon-exon splice junctions.
Consistent quality and adapter trimming for RRBS or standard FastQ files
Trimmomatic: A flexible read trimming tool for Illumina NGS data
