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Showing 20 out of 28,684 Resources on page 1384

PersMed

Life science consultancy and analysis service company. Analysis services include microarray analysis, next generation sequencing, experiment design, and biostatistics. Consultancy centers around experimental design in approaches involving large sets of patient-derived data.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

DTU Multi-Assay Core

Facility for performing and analyzing high-throughput biological assays. The facility provides advice and research service with a range of high-throughput assays. Analysis of microarrays, sequencing, QPCR, and flow cytometry are provided.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

Translational Research Laboratory

Cancer research laboratory at the Peter MacCallum Cancer Centre which investigates biomarkers identification, compounds for activity as anti-cancer drugs, and small molecule targeted therapies.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

University of Oxford Labs and Facilities

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on April 15,2024. An independent portal that lists the labs and facilities at the University of Oxford.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

Reveal Biosciences

Contract research organization (CRO) that specializes in advanced tissue technologies. It offers services in histology, immunohistochemistry, digital pathology, and image analysis.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

RPCI Gene Targeting and Transgenic Shared Resource

Facility which provides researchers with transgenic mouse technologies, methods, and animal models. Knockout mice, transgenic mice, and mice on multiple strain backgrounds are provided.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

Illuminator

A sequence alignment program for the output from Illumina GA-II clonal sequencers. It uses an algorithm that indexes the reference sequence as a series of 8-mers and then matches the genomic reads to the 8-mer index, in a mutation-tolerant way permitting identification of single-nucleotide substitutions and indels.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

MassGenomics

Blog discussing next-generation sequencing and medical genomics in the post-genome era. Most posts are in-depth reviews of recent research publications or editorials.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

Phred

A base calling program for DNA sequence traces.

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  • SciCrunch
  • 13 years ago - by Anonymous

Geoffs Bio-Directories

A comprehensive listing of companies and organizations involved with genomics and molecular biology. There are lists for genome software and services, genome institutions and supplies, and general institutions.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

FUSIM

A software tool for simulating fusion transcripts from a reference genome.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

NPEBseq

A method for non-parametric, empirical Bayesian-based analysis of RNA-seq count data.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

ASC

Borrows information across sequences to establish prior distribution of sample variation, so that biological variation can be accounted for even when replicates are not available.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

SplitSeek

THIS RESOURCE IS NO LONGER IN SERVICE, documented September 20, 2016. A program for de novo prediction of splice junctions in RNA-seq data.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

Google Compute Engine

An infrastructure as a service that lets you run your large-scale computing workloads on Linux virtual machines hosted on Google's infrastructure.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

BLASTP

Data analysis service whose programs search protein databases using a protein query. The algorithms used include blastp, psi-blast, phi-blast, and delta-blast.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

PREFAB

Downloadable data designed for testing multiple sequence alignment methods.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

GRS

A compression tool for efficient storage of Genome Re-Sequencing data. GRS processes genome sequence data without use of reference SNPs and other variants. It can also automatically rebuild the individual genome sequence data using the reference genome sequence.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

GDC

A C++ application designed for compression of genome collections from the same species.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous

fastqz

Source code used to compress FASTQ files. FASTQ is DNA sequencing machine output.

  • Resource
  • SciCrunch
  • 13 years ago - by Anonymous