X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

Search Again

We support boolean queries, use +,-,<,>,~,* to alter the weighting of terms

Showing 20 out of 29,158 Resources on page 913

Aroma.affymetrix

An R package for analyzing large Affymetrix data sets.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

Agilent Genomic Workbench

A comprehensive design and analysis tool for setting up and interpreting your microarray experiments.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

Agilent CytoGenomics software

Software for a complete CGH and CGH+SNP microarray data analysis and data reporting solution to streamline the day-to-day cytogenetic sample analysis research workflow.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

ADaCGH

A web tool for the analysis of aCGH data sets. They focus on calling gains and losses and estimating the number of copy changes. Note: ADaCGH will continue being maintained, but is deprecated. Their new tool for CGH and CNV is WaviCGH, http://wavi.bioinfo.cnio.es/

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

aCGHtool

A software tool for the normalization, visualization, breakpoint detection, and comparative analysis of array-CGH data which allows the accurate and sensitive detection of CNAs.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

SEAL

A suite of distributed software applications for aligning short DNA reads, and manipulating and analyzing short read alignments.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

PPSEQ

A software suite including a scalable hierarchical multitasking parallel infrastructure and the classical sequencing algorithms.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

ERNE

A short string alignment package whose goal is to provide an all-inclusive set of tools to handle short (NGS-like) reads.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

CloudBurst

A new parallel read-mapping algorithm optimized for mapping next-generation sequence data to the human genome and other reference genomes, for use in a variety of biological analyses including SNP discovery, genotyping, and personal genomics.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

BWA

Software for aligning sequencing reads against large reference genome. Consists of three algorithms: BWA-backtrack, BWA-SW and BWA-MEM. First for sequence reads up to 100bp, and other two for longer sequences ranged from 70bp to 1Mbp.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

Genomic HyperBrowser

A generic web-based system, providing statistical methodology and computing power to handle a variety of biological inquires on genomic datasets.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

MethMarker

Tool that facilitates the design and optimization of gene-specific DNA methylation assays. Beyond its use as an epigenetic primer-design tool, it provides extensive support for epigenetic biomarker optimization. Download MethMarker or start it directly from within your web browser.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

QUMA

You can easily align, visualize and quantify bisulfite sequence data for CpG methylation analysis.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

BatMeth

Improved mapper for bisulfite sequencing reads on DNA methylation.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

B-SOLANA

An approach for the analysis of two-base encoding bisulfite sequencing data.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

MeRIP-PF

A high-efficiency and easy-to-use analysis pipeline for MeRIP-Seq peak-finding at high resolution, which compares distributions of reads between immunoprecipitation sample and control sample.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

Piranha

A peak-caller for CLIP- and RIP-Seq data. It takes input in BED or BAM format and identifies regions of significant read enrichment. Additional covariates may optionally be provided to further inform the peak-calling process., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

mCarts

A hidden Markov model (HMM)-based software to predict clusters RNA motif sites.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

TreeTFDB

A public database that provides the complete transcription factor (TF) repertoires of 6 genome sequenced tree species: papaya (Carica papaya), jatoropha (Jatropha curcas), cassava (Manihot esculenta), poplar (Populus trichocarpa), castor bean (Ricinus communis) and grape vine (Vitis vinifera). from annotated genes on each genome.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

SoyDB

A Knowledge Database of Soybean Transcription Factors. PSI-BLAST is available to find hits from the database.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous