1. SAMtools
Various utilities for processing alignments in the SAM format, including variant calling and alignment viewing. SAM Tools provide various utilities for manipulating alignments in the SAM format, including sorting, merging, indexing and generating alignments in a per-position format. ...
标签:SNP discovery
2. Maq
Mapping and Assembly with Qualities (renamed from MAPASS2). Particularly designed for Illumina-Solexa 1G Genetic Analyzer, and has preliminary functions to handle ABI SOLiD data. Maq stands for Mapping and Assembly with Quality. It builds assembly by mapping short reads to reference ...
标签:Genomics, SNP discovery
3. SOAP
SOAP (Short Oligonucleotide Alignment Program) is a program for efficient gapped and ungapped alignment of short oligonucleotides onto reference sequences. SOAP2 is an updated program based on Burrows-Wheeler Transform. has been in evolution from a single alignment tool to a tool pac...
标签:SNP discovery
4. GATK
The Genome Analysis Toolkit (GATK) is a structured programming framework designed to enable rapid development of efficient and robust analysis tools for next-generation DNA sequencers. The GATK solves the data management challenge by separating data access patterns from analysis algorit...
标签:SNP discovery
5. MIRA
MIRA 3 - Whole Genome Shotgun and EST Sequence Assembler Whole Genome Shotgun and EST sequence assembler
标签:De-novo assembly, SNP discovery, RNA-Seq Alignment
6. SOAPsnp
SOAPsnp is an accurate consensus sequence builder based on soap1 and SOAPaligner/soap2's alignment output. It calculates a quality score for each consensus base, which can be used for any latter process to call SNPs.
标签:SNP discovery
7. Shore
Analysis suite for short read data.
标签:Structural variation, SNP discovery
8. VarScan
VarScan, an open source tool for variant detection that is compatible with several short read align-ers.
标签:SNP discovery
9. ERGO Genome Analysis and Discovery System
ERGO provides a systems-biology informatics toolkit centered on comparative genomics to capture, query and visualize sequenced genomes. Building upon the most comprehensive genomic database available anywhere integrated with the largest collection of microbial metabolic and non-metaboli...
标签:Metabolic reconstruction,Phylogenetics, Comparative genomics, SNP Annotation, SNP discovery, Alignment, Exome analysis, Metagenomics,Pathway analysis, Comparative transcriptomics, Functional Genomics, Gene Expression Analysis, Genome Wide Association Stud
10. CLCbio Genomics Workbench
De novo and reference assembly SNP and small indel detection and annotation.
标签:Genomics, Whole Genome Resequencing, De-novo assembly, SNP discovery, InDel discovery, ChIP-Seq, RNA-Seq,MiRNA, Transcriptomics
11. SeqMan NGen
Sequence assembly software using traditional, next-gen, and third-gen techonologies. Subsequent analysis of the assembly, including SNP discovery, coverage evaluation and consensus annotation is provided through full integration with Lasergene.
标签:Genomics, De-novo assembly, De novo transcriptome assembly,Whole Genome Resequencing, SNP discovery, InDel discovery,ChIP-Seq, RNA-Seq Alignment
12. Syzygy
Software to identify variants from pooled sequencing data
标签:SNP discovery, InDel discovery
13. PyroBayes
PyroBayes is a novel base caller for pyrosequences from the 454 Life Sciences sequencing machines.
标签:SNP discovery
14. Crossbow
Crossbow is a cloud-computing software tool that combines the aligner BOWTIE and the SNP caller SOAPsnp. Crossbow is a cloud-computing software tool that combines the aligner BOWTIE and the SNP caller SOAPsnp.
标签:SNP discovery
15. SNPSeeker
Identification of SNPs in pooled genomic samples
标签:SNP discovery
16. Trans-ABySS
Trans-ABySS is a software package that is designed to analyze ABySS-assembled whole-genome shotgun transcriptome data.
标签:RNA-Seq, SNP discovery, Fusion genes, InDel discovery, Fusion transcripts
17. CloudBurst
CloudBurst is a parallel read-mapping algorithm optimized for mapping next-generation sequence data to the human genome and other reference genomes.
标签:SNP discovery, Genotyping,Personal genomics
18. SNVMix
Detects single nucleotide variants from next generation sequencing data.
标签:SNP discovery
19. Atlas-SNP2
Atlas-SNP2 is a SNP discovery tool developed for next generation sequencing platforms
标签:SNP discovery
20. SNIP-Seq
Tool for discovering SNPs in population sequencing data
标签:SNP discovery