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http://bioinformatics.rutgers.edu/Software/SLiQ/

Software for simple linear inequalities based Mate-Pair reads filtering and scaffolding. A set of simple linear inequalities (SLIQ) derived from the geometry of contigs on the line that can be used to predict the relative positions and orientations of contigs from individual mate pair reads and thus produce a contig digraph. The SLIQ inequalities can also filter out unreliable mate pairs and can be used as a pre-processing step for any scaffolding algorithm. This tool filters mate pairs and then produces a Directed Contig Graph (contig diGraph). Also provided is a Naive scaffolder that can then produce scaffolds out of the contig diGraph.

Proper citation: SLIQ (RRID:SCR_005003) Copy   

•   Source: SciCrunch Registry

http://cortexassembler.sourceforge.net/index_cortex_var.html

A tool for genome assembly and variation analysis from sequence data. You can use it to discover and genotype variants on single or multiple haploid or diploid samples. If you have multiple samples, you can use Cortex to look specifically for variants that distinguish one set of samples (eg phenotype=X, cases, parents, tumour) from another set of samples (eg phenotype=Y, controls, child, normal). cortex_var features * Variant discovery by de novo assembly - no reference genome required * Supports multicoloured de Bruijn graphs - have multiple samples loaded into the same graph in different colours, and find variants that distinguish them. * Capable of calling SNPs, indels, inversions, complex variants, small haplotypes * Extremely accurate variant calling - see our paper for base-pair-resolution validation of entire alleles (rather than just breakpoints) of SNPs, indels and complex variants by comparison with fully sequenced (and finished) fosmids - a level of validation beyond that demanded of any other variant caller we are aware of - currently cortex_var is the most accurate variant caller for indels and complex variants. * Capable of aligning a reference genome to a graph and using that to call variants * Support for comparing cases/controls or phenotyped strains * Typical memory use: 1 high coverage human in under 80Gb of RAM, 1000 yeasts in under 64Gb RAM, 10 humans in under 256 Gb RAM

Proper citation: cortex var (RRID:SCR_005081) Copy   

•   Source: SciCrunch Registry

http://www.appliedbiosystems.com/absite/us/en/home.html

An Antibody supplier

Proper citation: Applied Biosystems (RRID:SCR_005039) Copy   

•   Source: SciCrunch Registry

http://www.physics.rutgers.edu/~anirvans/SOPRA/

Software tool to exploit the mate pair/paired-end information for assembly of short reads from high throughput sequencing platforms, e.g. Illumina and SOLiD.

Proper citation: SOPRA (RRID:SCR_005035) Copy   

•   Source: SciCrunch Registry

https://www.bioworlde.com/

An Antibody supplier

Proper citation: Bioworld Technology (RRID:SCR_005036) Copy   

•   Source: SciCrunch Registry

http://www.giftofhope.org/

Gift of Hope Organ & Tissue Donor Network is proud to serve as the federally designated not-for-profit agency that coordinates organ and tissue donation and supports families of donors in the northern three-quarters of Illinois and northwest Indiana. Since our inception in 1986, we have coordinated donations that have saved the lives of 17,000 organ transplant recipients and helped hundreds of thousands of other patients receive needed tissue transplants. As one of 58 organ procurement organizations (OPOs) that make up the nation''s organ donation system, we work with 179 hospitals in our donation service area. In managing the recovery, care and transportation of donated organs to transplant patients, we work closely with Illinois'' nine transplant centers, which operate 32 transplant programs. We also work with other transplant centers and other OPOs through the United Network for Organ Sharing (UNOS) to provide lifesaving organs for patients awaiting them. UNOS is the federally mandated registration center for organ transplant candidates in the United States. UNOS'' computer-based system matches donated organs with patients in need, in accordance with strict federal guidelines intended to ensure equitable distribution.

Proper citation: Gift of Hope Organ and Tissue Donor Network (RRID:SCR_004968) Copy   

•   Source: SciCrunch Registry

http://www.baseclear.com/landingpages/basetools-a-wide-range-of-bioinformatics-solutions/sspacev12/

A stand-alone software program for scaffolding pre-assembled contigs using paired-read data. Main features are: a short runtime, multiple library input of paired-end and/or mate pair datasets and possible contig extension with unmapped sequence reads.

Proper citation: SSPACE (RRID:SCR_005056) Copy   

•   Source: SciCrunch Registry

http://meringlab.org/software/hpc-clust/

A set of tools designed to cluster large numbers (>1 million) of pre-aligned nucleotide sequences. It performs the clustering of sequences using the Hierarchical Clustering Algorithm (HCA). There are currently three different cluster metrics implemented: single-linkage, complete-linkage, and average-linkage. In addition, there are currently four sequence distance functions implemented, these are: identity (gap-gap counting as match), nogap (gap-gap being ignored), nogap-single (like nogap, but consecutive gap-nogap''s count as a single mismatch), tamura (distance is calculated with the knowledge that transitions are more likely than transversions). One advantage that HCA has over other algorithms is that instead of producing only the clustering at a given threshold, it produces the set of merges occuring at each threshold. With this approach, the clusters can afterwards very quickly be reported for every arbitrary threshold with little extra computation. This approach also allows the plotting of the variation of number of clusters with clustering threshold without requiring the clustering to be run for each threshold independently. Another feature of the way HPC-CLUST is implemented is that the single-, complete-, and average-linkage clusterings can be computed in a single run with little overhead.

Proper citation: HPC-CLUST (RRID:SCR_005052) Copy   

•   Source: SciCrunch Registry

http://plaza.ufl.edu/xywang/Mpick.htm

A modularity-based clustering software for Operational Taxonomic Unit (OTU) picking of 16S rRNA sequences. The algorithm does not require a predetermined cut-off level, and our simulation studies suggest that it is superior to existing methods that require specified distance or variance levels to define OTUs.

Proper citation: M-pick (RRID:SCR_004995) Copy   

•   Source: SciCrunch Registry

http://www.manchester.ac.uk/

Public research university in Manchester, England, formed in 2004 by merger of University of Manchester Institute of Science and Technology and Victoria University of Manchester. Second largest university in United Kingdom by enrollment.

Proper citation: University of Manchester; Manchester; United Kingdom (RRID:SCR_004996) Copy   

•   Source: SciCrunch Registry

https://bxcell.com/

Commercial supplier and developer of in vivo antibodies. Provides antibodies and antibody production services.

Proper citation: Bio X Cell (RRID:SCR_004997) Copy   

•   Source: SciCrunch Registry

http://plaza.ufl.edu/sunyijun/ES-Tree.htm

Software for hierarchical Clustering Analysis of Millions of 16S rRNA Pyrosequences in Quasi-linear Time.

Proper citation: ESPRIT-Tree (RRID:SCR_005045) Copy   

•   Source: SciCrunch Registry

http://english.hust.edu.cn/

Public research university located in Guanshan Subdistrict, Hongshan District, Wuhan, Hubei province, China.

Proper citation: Huazhong University of Science and Technology; Wuhan; China (RRID:SCR_005047) Copy   

•   Source: SciCrunch Registry

http://www.cuni.cz/UKEN-1.html

Research university located in Prague, Czech Republic.

Proper citation: Charles University; Prague; Czech Republic (RRID:SCR_002931) Copy   

•   Source: SciCrunch Registry

http://www.genox.com

Biotechnological company that produces and supplies materials to oxidative stress and aging researchers.

Proper citation: Genox Corpooration (RRID:SCR_002930) Copy   

•   Source: SciCrunch Registry

http://biohealth.snu.ac.kr/software/TRAP/

A comprehensive software package integrating all necessary tasks such as mapping short reads, measuring gene expression levels, finding differentially expressed genes (DEGs), clustering and pathway analysis for time-series data in a single environment.

Proper citation: Time-series RNA-seq Analysis Package (RRID:SCR_002935) Copy   

•   Source: SciCrunch Registry

http://www.genscript.com

Commercial organization which provides life science services and products to researchers. They specialize in gene synthesis, peptide, protein, antibody and preclinical drug development service.

Proper citation: GenScript (RRID:SCR_002891) Copy   

•   Source: SciCrunch Registry

http://pfind.ict.ac.cn/software/pBuild/index.html

A software tool that can compare several search engines' results and combine them together.

Proper citation: pBuild (RRID:SCR_002929) Copy   

•   Source: SciCrunch Registry

http://www.nationalpostdoc.org/

Representative organization for postdoctoral scholars in the United States. It is member-driven and non-profit.

Proper citation: National Postdoctoral Association (RRID:SCR_002928) Copy   

•   Source: SciCrunch Registry

http://cran.r-project.org/src/contrib/Archive/aCGH.Spline/

An R package for array comparative genomic hybridization (aCGH) dye bias normalization.

Proper citation: aCGH.Spline (RRID:SCR_002927) Copy   

•   Source: SciCrunch Registry