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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.
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.
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.
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.
Contract research organization (CRO) that specializes in advanced tissue technologies. It offers services in histology, immunohistochemistry, digital pathology, and image analysis.
Facility which provides researchers with transgenic mouse technologies, methods, and animal models. Knockout mice, transgenic mice, and mice on multiple strain backgrounds are provided.
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.
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.
A base calling program for DNA sequence traces.
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.
A software tool for simulating fusion transcripts from a reference genome.
A method for non-parametric, empirical Bayesian-based analysis of RNA-seq count data.
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.
THIS RESOURCE IS NO LONGER IN SERVICE, documented September 20, 2016. A program for de novo prediction of splice junctions in RNA-seq data.
An infrastructure as a service that lets you run your large-scale computing workloads on Linux virtual machines hosted on Google's infrastructure.
Data analysis service whose programs search protein databases using a protein query. The algorithms used include blastp, psi-blast, phi-blast, and delta-blast.
Downloadable data designed for testing multiple sequence alignment methods.
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.
A C++ application designed for compression of genome collections from the same species.
Source code used to compress FASTQ files. FASTQ is DNA sequencing machine output.