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SciCrunch Registry is a curated repository of scientific resources, with a focus on biomedical resources, including tools, databases, and core facilities - visit SciCrunch to register your resource.
| Resource Name | Proper Citation | Abbreviations | Resource Type |
Description |
Keywords | Resource Relationships | ||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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MADAM Resource Report Resource Website |
MADAM (RRID:SCR_001216) | MADAM | data management software, software application, software resource | THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 23,2022.Data management software implemented in Java that facilitates the entry of data into a relational database. It guides users through the microarray process from RNA procurement to data analysis, offering intelligent forms to simplify the tracking of experimental parameters and results that are essential for the interpretation of expression results in downstream analyses. Canned reports provide information on RNA samples, studies, slide maps and other pertinent data and a general SQL query window allows freeform access to the underlying database. MADAM also serves as a platform for launching other data entry and management tools. Through the use of these integrated modules, users can view and score PCR plates, design experiments and studies, and track laboratory materials. | microarray, data management software, rna |
is listed by: OMICtools is related to: MicroArray and Gene Expression Markup Language has parent organization: TM4 |
PMID:20193058 | THIS RESOURCE IS NO LONGER IN SERVICE | OMICS_02127 | SCR_001216 | SciCrunch Registry | MADAM (TM4 Microarray Software Suite), TM4 Microarray Software Suite: MicroArray DAta Manager, MADAM: MicroArray DAta Manager, TM4 Microarray Software Suite: MADAM, MicroArray DAta Manager, TM4 MADAM | 2026-10-24 12:44:29 | 0 | ||||||
|
Microarray Data Analysis System Resource Report Resource Website 1+ mentions |
Microarray Data Analysis System (RRID:SCR_001218) | MIDAS | software resource | Application that provides users an interface to design analysis protocols combining one or more normalization and filtering steps. In this way, data from many individual hybridizations can be treated in a uniform and reproducible manner. | microarray, normalization, windows, mac osx, linux, java |
is listed by: OMICtools has parent organization: TM4 |
Artistic License | OMICS_02126 | https://sourceforge.net/projects/midas-tm4/ | http://www.tm4.org/midas.html | SCR_001218 | SciCrunch Registry | TM4 Microarray Software Suite: Microarray Data Analysis System, TM4 Microarray Software Suite: MIDAS, MIDAS (TM4 Microarray Software Suite), TM4 MIDAS, MIDAS: Microarray Data Analysis System | 2026-10-24 12:44:28 | 4 | |||||
|
globaltest Resource Report Resource Website 10+ mentions |
globaltest (RRID:SCR_001256) | globaltest | data analysis software, data processing software, sequence analysis software, software application, software resource | A software package that tests groups of covariates (or features) for association with a response variable. The package implements the test with diagnostic plots and multiple testing utilities, along with several functions to facilitate the use of this test for gene set testing of GO and KEGG terms. | differential expression, go, microarray, one channel, pathway, bio.tools |
uses: KEGG is listed by: OMICtools is listed by: Debian is listed by: bio.tools is related to: Gene Ontology has parent organization: Bioconductor |
PMID:34046931 | Free, Available for download, Freely available | biotools:globaltest, OMICS_02084 | https://bio.tools/globaltest | SCR_001256 | SciCrunch Registry | 2026-10-24 12:44:32 | 31 | ||||||
|
iterativeBMAsurv Resource Report Resource Website |
iterativeBMAsurv (RRID:SCR_001254) | iterativeBMAsurv | software resource | Software package providing a variable selection method for applying survival analysis to microarray data. | microarray |
is listed by: OMICtools has parent organization: Bioconductor |
PMID:19245714 | GNU General Public License, v2 or newer | OMICS_02086 | SCR_001254 | SciCrunch Registry | The Iterative Bayesian Model Averaging (BMA) Algorithm For Survival Analysis, iterativeBMAsurv - The Iterative Bayesian Model Averaging (BMA) Algorithm For Survival Analysis | 2026-10-24 12:44:30 | 0 | ||||||
|
snpStats: SnpMatrix and XSnpMatrix classes and methods Resource Report Resource Website 50+ mentions |
snpStats: SnpMatrix and XSnpMatrix classes and methods (RRID:SCR_001249) | snpStats | software resource | Software for classes and statistical methods for large single nucleotide polymorphism (SNP) association studies. | r, single nucleotide polymorphism, genetic variability, microarray |
is listed by: OMICtools has parent organization: Bioconductor has parent organization: University of Cambridge; Cambridge; United Kingdom |
PMID:16720584 | Free, Available for download, Freely available | OMICS_02091 | SCR_001249 | SciCrunch Registry | 2026-10-24 12:44:28 | 79 | |||||||
|
piCALL Resource Report Resource Website 1+ mentions |
piCALL (RRID:SCR_001242) | piCALL | software resource | Software to detect short insertion / deletion variants (and SNPs) from population sequence data, i.e. sequence reads generated from a population of individuals. It uses a probabilistic model to utilize sequence reads from a population of individuals to automatically account for context-specific sequencing errors associated with indels. piCALL is implemented in C for use on Linux platforms and can be applied to sequence data from different sequencing platforms. However, the method requires each individual in a dataset to be sequenced using the same platform. The reads for each individual should be aligned to the same reference genome sequence. Note that the program will not be able to call indels from individual sequence datasets or data from a small number of individuals. | c, genotyping, indel, population, high-throughput sequencing, insertion, deletion, variant, single nucleotide polymorphism, linux, bio.tools |
is listed by: OMICtools is listed by: bio.tools is listed by: Debian has parent organization: Scripps Research Institute |
PMID:21653520 | OMICS_02098, biotools:picall | https://bio.tools/picall | http://polymorphism.scripps.edu/~vbansal/software/piCALL/ | SCR_001242 | SciCrunch Registry | 2026-10-24 12:44:28 | 1 | ||||||
|
mapDamage Resource Report Resource Website 100+ mentions |
mapDamage (RRID:SCR_001240) | mapDamage | software resource | Software for tracking and quantifying DNA damage patterns among ancient DNA sequencing reads generated by Next-Generation Sequencing platforms. | python, r, illumina, windows, perl, dna damage, dna sequencing, next-generation sequencing, dna, bio.tools |
is listed by: OMICtools is listed by: bio.tools is listed by: Debian has parent organization: University of Copenhagen; Copenhagen; Denmark |
PMID:23613487 PMID:21659319 DOI:10.1093/bioinformatics/btt193 |
Free, Available for download, Freely available | OMICS_02099, biotools:mapdamage | https://bio.tools/mapdamage, https://sources.debian.org/src/mapdamage/ | SCR_001240 | SciCrunch Registry | mapDamage 2.0, mapDamage: tracking and quantifying damage patterns in ancient DNA sequences, mapDamage2.0 | 2026-10-24 12:44:27 | 395 | |||||
|
KMC Resource Report Resource Website 10+ mentions |
KMC (RRID:SCR_001245) | KMC | software resource | Software utility for counting k-mers (sequences of consecutive k symbols) in a set of reads from genome sequencing projects. It scans the raw reads and produces a compact representation of all non-unique reads accompanied with number of their occurrences. The algorithm implemented makes use mostly of disk space rather than RAM, which allows to use KMC even on rather typical personal computers. | c++, k-mer, genome sequencing, linux, windows, de bruijn graph |
is listed by: OMICtools is listed by: Debian has parent organization: Silesian University of Technology; Silesia; Poland |
PMID:23679007 DOI:10.1093/bioinformatics/btv022 |
Free, Available for download, Freely available | OMICS_02095 | https://sources.debian.org/src/kmc/ | SCR_001245 | SciCrunch Registry | KMC - K-mer Counter, K-mer Counter | 2026-10-24 12:44:27 | 10 | |||||
|
DSK Resource Report Resource Website 1+ mentions |
DSK (RRID:SCR_001246) | DSK | software resource | A k-mer counting software that can count k-mers of large Illumina datasets on laptops and desktop computers. | illumina, k-mer, bio.tools |
is listed by: OMICtools is listed by: bio.tools is listed by: Debian |
PMID:23325618 | Free, Freely available | biotools:dsk, OMICS_02094 | https://bio.tools/dsk | SCR_001246 | SciCrunch Registry | disk streaming of k-mers, DSK: disk streaming of k-mers | 2026-10-24 12:44:29 | 1 | |||||
|
ChIP-seq Resource Report Resource Website 5000+ mentions |
ChIP-seq (RRID:SCR_001237) | ChIP-seq | data analysis software, data processing software, software application, software resource, software toolkit | Set of software modules for performing common ChIP-seq data analysis tasks across the whole genome, including positional correlation analysis, peak detection, and genome partitioning into signal-rich and signal-poor regions. The tools are designed to be simple, fast and highly modular. Each program carries out a well-defined data processing procedure that can potentially fit into a pipeline framework. ChIP-Seq is also freely available on a Web interface. | high-throughput sequencing, chromatin immuno precipitation, chip-seq, genome, c |
is listed by: OMICtools has parent organization: SourceForge has parent organization: Ecole Polytechnique Federale de Lausanne; Lausanne; Switzerland has parent organization: SIB Swiss Institute of Bioinformatics |
PMID:27863463 | Free, Available for download, Freely available | OMICS_02103 | https://epd.expasy.org/chipseq/, https://chip-seq.sourceforge.net/ | SCR_001237 | SciCrunch Registry | ChIP-seq - Tools for the analysis of ChIP-seq data | 2026-10-24 12:44:28 | 8035 | |||||
|
exomeCopy Resource Report Resource Website 10+ mentions |
exomeCopy (RRID:SCR_001276) | exomeCopy | software resource | Software package for detection of copy number variants (CNV) from exome sequencing samples, including unpaired samples. The package implements a hidden Markov model which uses positional covariates, such as background read depth and GC-content, to simultaneously normalize and segment the samples into regions of constant copy count. | copy number variation, genetics, sequencing, exome |
is listed by: OMICtools has parent organization: Bioconductor |
PMID:23089826 | Free, Available for download, Freely available | OMICS_02062 | http://www.bioconductor.org/packages/release/bioc/html/exomeCopy.html | SCR_001276 | SciCrunch Registry | exomeCopy - Copy number variant detection from exome sequencing read depth | 2026-10-24 12:44:28 | 16 | |||||
|
SMAP Resource Report Resource Website 100+ mentions |
SMAP (RRID:SCR_001270) | SMAP | software resource | Software package providing functions and classes for DNA copy number profiling of array-CGH data. | copy number variation, microarray, two channel |
is listed by: OMICtools has parent organization: Bioconductor |
PMID:18204059 | Free, Available for download, Freely available | OMICS_02068 | SCR_001270 | SciCrunch Registry | SMAP - A Segmental Maximum A Posteriori Approach to Array-CGH Copy Number Profiling | 2026-10-24 12:44:28 | 210 | ||||||
|
SNAGEE Resource Report Resource Website |
SNAGEE (RRID:SCR_001301) | SNAGEE | software resource | Software package that uses signal-to-noise ratios (SNRs) as a proxy for quality of gene expression studies and samples. The SNRs can be calculated on any gene expression data set as long as gene IDs are available, no access to the raw data files is necessary. This allows to flag problematic studies and samples in any public data set. | microarray, one channel, quality control, two channel, gene expression |
is listed by: OMICtools has parent organization: Bioconductor |
PMID:23251415 | Free, Available for download, Freely available | OMICS_02035 | SCR_001301 | SciCrunch Registry | Signal-to-Noise applied to Gene Expression Experiments | 2026-10-24 12:44:29 | 0 | ||||||
|
MinimumDistance Resource Report Resource Website |
MinimumDistance (RRID:SCR_001260) | MinimumDistance | data analysis software, data processing software, software application, software resource | Software package for analysis of de novo copy number variants in trios from high-dimensional genotyping platforms. | copy number variation, microarray, snp |
is listed by: OMICtools has parent organization: Bioconductor |
Free, Available for download, Freely available | OMICS_02066 | SCR_001260 | SciCrunch Registry | MinimumDistance - A package for de novo CNV detection in case-parent trios | 2026-10-24 12:44:32 | 0 | |||||||
|
Local Ancestry in adMixed Populations Resource Report Resource Website 1+ mentions |
Local Ancestry in adMixed Populations (RRID:SCR_001258) | LAMP | software resource | A software package for the inference of locus-specific ancestry in recently admixed populations. LAMP-LD takes the genotypes of admixed individuals as well as reference haplotype panels approximating the mixing ancestral populations, and outputs the estimated number of alleles from each ancestry in each locus for each individual. The LAMP-LD package also includes the program LAMP-HAP, which processes haplotype data when high-quality phasing is available, and utilizes trio nuclear family designs to improve estimation accuracy. LAMP-LD is based on a window-based processing combined within a hierarchical Hidden Markov Model. It can process 2,3 or 5 mixing populations, and its short per-sample processing time makes it suitable for analyzing large datasets of dense SNP panels. The original program LAMP does not use the LD and therefore is not as accurate, but it is useful in cases where the SNP density is not high enough or when the ancestral haplotypes are unkown. | locus, ancestry, admixed, population, genotype, haplotype, allele | is listed by: OMICtools | NSF 513599 | PMID:22495753 PMID:19477991 PMID:18252211 |
THIS RESOURCE IS NO LONGER IN SERVICE | OMICS_02080 | SCR_001258 | SciCrunch Registry | 2026-10-24 12:44:30 | 9 | ||||||
|
factDesign Resource Report Resource Website |
factDesign (RRID:SCR_001330) | factDesign | data analysis software, data processing software, software application, software resource | Software package that provides a set of tools for analyzing data from a factorial designed microarray experiment, or any microarray experiment for which a linear model is appropriate. The functions can be used to evaluate tests of contrast of biological interest and perform single outlier detection. | microarray, differential expression |
is listed by: OMICtools has parent organization: Bioconductor |
PMID:18584033 | Free, Available for download, Freely available | OMICS_02008 | SCR_001330 | SciCrunch Registry | factDesign - Factorial designed microarray experiment analysis | 2026-10-24 12:44:31 | 0 | ||||||
|
NGSrich Resource Report Resource Website 10+ mentions |
NGSrich (RRID:SCR_001333) | software resource | Software for target enrichment performance for next-generation sequencing. | standalone software, java, bio.tools |
is listed by: OMICtools is listed by: bio.tools is listed by: Debian has parent organization: SourceForge |
PMID:22290614 | Free, Available for download, Freely available | OMICS_03603, biotools:ngsrich | https://bio.tools/ngsrich | SCR_001333 | SciCrunch Registry | 2026-10-24 12:44:30 | 10 | |||||||
|
pickgene Resource Report Resource Website |
pickgene (RRID:SCR_001331) | pickgene | data analysis software, data processing software, software application, software resource | Software for adaptive Gene Picking for Microarray Expression Data Analysis. | microarray, gene expression, differential expression, bio.tools |
is listed by: OMICtools is listed by: Debian is listed by: bio.tools has parent organization: Bioconductor |
Free, Available for download, Freely available | OMICS_02007, biotools:pickgene | https://bio.tools/pickgene | SCR_001331 | SciCrunch Registry | 2026-10-24 12:44:29 | 0 | |||||||
|
oneChannelGUI Resource Report Resource Website 10+ mentions |
oneChannelGUI (RRID:SCR_001325) | oneChannelGUI | software resource | Software library that provides a graphical interface for microarray gene and exon level analysis as well as miRNA/mRNA-seq data analysis. The package was developed to simplify the use of Bioconductor tools for beginners having limited or no experience in writing R code. | differential expression, gui, microarray, multiple comparison, preprocessing, quality control, rna-seq, exon, bio.tools |
is listed by: OMICtools is listed by: bio.tools is listed by: Debian has parent organization: Bioconductor |
PMID:17875544 | Free, Available for download, Freely available | biotools:onechannelgu, OMICS_02004 | http://www.bioconductor.org/packages/release/bioc/html/oneChannelGUI.html | SCR_001325 | SciCrunch Registry | 2026-10-24 12:44:30 | 13 | ||||||
|
CYCLE Resource Report Resource Website 1+ mentions |
CYCLE (RRID:SCR_001328) | CYCLE | software resource | Software package for the identification of periodically expressed genes using Fourier analysis and the statistical assessment of significance using different background models. | r, microarray, time course, periodic expression pattern, time-series, bio.tools |
is listed by: OMICtools is listed by: bio.tools is listed by: Debian has parent organization: Humboldt University of Berlin; Berlin; Germany has parent organization: Bioconductor |
PMID:18310054 | THIS RESOURCE IS NO LONGER IN SERVICE | OMICS_02010, biotools:cycle | http://www.bioconductor.org/packages/release/bioc/html/cycle.html, https://bio.tools/cycle | SCR_001328 | SciCrunch Registry | 2026-10-24 12:44:33 | 4 |
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