Curator Dashboard

A genome browser specialized in next-generation sequencing data.

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• SciCrunch
• 13 years ago - by Anonymous

Software for decoding error-correcting barcodes.

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• SciCrunch
• 13 years ago - by Anonymous

Software to generate a visual representation of sRNAs and user-imported genomic features. The tool may be run on its own or from other tools, e.g. miRCat.

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• SciCrunch
• 13 years ago - by Anonymous

A platform and application suite for bringing together omics and clinical data.

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• SciCrunch
• 13 years ago - by Anonymous

Software for detecting differential features across the entire spectrum, including the lower counts.

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• SciCrunch
• 13 years ago - by Anonymous

Software using a statistical approach, based on a two-stage Poisson model, for modeling RNA sequencing data and testing for biologically important changes in gene expression.

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• SciCrunch
• 13 years ago - by Anonymous

Software that calculates the coverage of high-throughput short-reads against a genome of reference and summarizes it per feature of interest (e.g. exon, gene, transcript). The data can be normalized as ''RPKM'' or by the ''DESeq'' or ''edgeR'' package.

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• SciCrunch
• 13 years ago - by Anonymous

A database that houses annotations of human splice isoforms. It adds reliable protein structural and functional data and information from cross-species conservation. A visual representation of the annotations for each gene allows users to easily identify functional changes brought about by splicing events. In addition to collecting, integrating and analyzing reliable predictions of the effect of splicing events, it also selects a single reference sequence for each gene, termed the principal isoform, based on the annotations of structure, function and conservation for each transcript.

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• SciCrunch
• 13 years ago - by Anonymous

Database that classifies human transcription factors based on the characteristics of their DNA-binding domains. It comprises six levels (superclasses, classes, families, subfamilies, genera and factor species), two of which are optional (subfamilies and factor species). The full classification can also be obtained as html document and as ontology in obo-format., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.

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• SciCrunch
• 13 years ago - by Anonymous

A public database holding PCR primers for popular DNA methylation analysis methods to prevent time-consuming primer design and experimental optimisation.

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• SciCrunch
• 13 years ago - by Anonymous

Software for automatic detection of absolute segmental copy numbers and genotype status in complex cancer genome profiles measured by single-nucleotide polymorphism (SNP) arrays. The method is based on pattern recognition of segmented and smoothed copy number and allelic imbalance profiles. The method performs well even for poor-quality data, low tumor content, and highly rearranged tumor genomes.

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• SciCrunch
• 13 years ago - by Anonymous

A database for histone mutations and their phenotypes.

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• SciCrunch
• 13 years ago - by Anonymous

A database of CpG islands and analytical tools for identifying comprehensive methylation profiles in cancer cells.

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• SciCrunch
• 13 years ago - by Anonymous

Datbase and web-based system for visualization and analysis of genome-wide methylation data of human cancers.

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• SciCrunch
• 13 years ago - by Anonymous

This blog reflects the workings of a group of scientists working at the intersection of public health microbiology and bioinformatics.

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• SciCrunch
• 13 years ago - by Anonymous

A blog about genetics, genomics, and medical research.

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• SciCrunch
• 13 years ago - by Anonymous

Online community for industry news and careers for life science professionals.

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• SciCrunch
• 13 years ago - by Anonymous

Community building portal that serves over 3,000 members from more than 70 countries by addressing scientific policies, providing access to high quality publications, organizing meetings, and serving as a portal to information about training, education, employment, etc.

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• SciCrunch
• 13 years ago - by Anonymous

Organization that serves the scientific and educational needs of bioinformatic practitioners and the general public. They develop and maintain computational resources to facilitate world-wide communications and collaborations between people of all educational and professional levels. They provide and promote open access to the materials and methods required for, and derived from, research, development and education.

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• SciCrunch
• 13 years ago - by Anonymous

A sequence verification pipeline where users can submit trace files to verify if a clone''s physical sequence matches its reference sequence.

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• SciCrunch
• 13 years ago - by Anonymous