21. CRISP
Identifies rare and common variants in pooled sequencing data
标签:SNP discovery
22. SOCS
SOLiD reference based, un-gapped alignment with bisulfite capability
标签:RNA-Seq Alignment, DNA methylation, SNP discovery
23. Slider
A new alignment approach that reduces the alignment problem space by utilizing each read base's probabilities given in the Illumina prb files.
标签:SNP discovery
24. MARGARITA
SNP discovery and genotyping from low-coverage sequencing data
标签:SNP discovery, Genotyping
25. PerM
PerM (Periodic Seed Mapping) uses periodic spaced seeds to significantly improve mapping efficiency for large reference genomes when compared to state-of-the-art programs.
标签:Genomics, SNP discovery
26. InGAP
inGAP is an integrated platform for next-generation sequencing project, the core function of which is to detect SNPs and indels using a Bayesian algorithm. Integrated Next-gen Genome Analysis Platform run with /biosoft/inGAP_linux64/inGAP
标签:SNP discovery
27. VAAL
VAAL is a variant ascertainment algorithm that can be used to detect SNPs, indels, and more complex genetic variants.
标签:Structural variation, SNP discovery, InDel discovery
28. Omixon Variant Toolkit
Omixon Target Standard, Target HLA and Target Pro are designed to help clinical, diagnostic and research labs to efficiently get the maximum accuracy and precision from their targeted NGS data.
标签:Comparative genomics, Mapping,Sequence analysis, Read alignment, InDel discovery,SNP discovery
29. SPLINTER
Identification of indel variants in pooled DNA with spike-in controls
标签:InDel discovery, SNP discovery
30. SRMA
SRMA is a short read micro re-aligner for next-generation high throughput sequencing data.
标签:SNP discovery, InDel discovery
31. PanGEA
Tool which enables a fast and user-friendly analysis of allele specific gene expression using the 454 technology.
标签:RNA-Seq, Allele-specific transcription, SNP discovery
32. DIAL
A computational pipeline for identifying single-base substitutions between two closely related genomes without the help of a reference genome.
标签:SNP discovery, Comparative genomics
33. ProbHD
We present a new strategy for identifying heterozygous sites in a single individual by using a machine learning approach that generates a heterozygosity score for each chromosomal position. Our approach also facilitates the identification of regions with unequal representation of two al...
标签:Population genetics, SNP discovery
34. Lasergene
Lasergene is a comprehensive DNA and protein sequence analysis software suite comprised of seven applications which include functions ranging from sequence assembly and SNP detection, to automated virtual cloning and primer design.
标签:Alignment, De novo sequencing,De-novo assembly, Genomics,InDel discovery, Integrated solution, Mapping,Phylogenetics, Protein structure analysis, Read alignment, SNP discovery,Sequence analysis,Transcription Factor Binding Site identification
35. SNVer
Variant calling in pooled or individual sequence data.
标签:SNP discovery
36. SNP-o-matic
SNP-o-matic is a fast, memory-efficient and stringent read mapping tool offering a variety of analytical output functions, with an emphasis on genotyping.
标签:SNP discovery
37. SeqEM
Genotype-calling algorithm that estimates parameters underlying the posterior probabilities in an adaptive way rather than arbitrarily specifying them a priori. The algorithm applies the well-known EM algorithm to an appropriate likelihood for a sample of unrelated individuals with next...
标签:SNP discovery
38. Atlas Suite
Atlas is a suite of variant analysis tools specializing in the separation of true SNPs and insertions and deletions (indels) from sequencing and mapping errors in Whole Exome Capture Sequecing (WECS) data. SNPs may be called using the Atlas-SNP2 application and indels may be called usin...
标签:SNP discovery, InDel discovery
39. Bambino
Variant detector and graphical alignment viewer for SAM/BAM format data.
标签:SNP discovery, Somatic mutations
40. ECHO
Reference-free short read error correction from diploid genomes, with explicit modeling of heterozygous sites.
标签:SNP discovery, InDel discovery