Bitnos is a free and collaborative Online Operating System that provides you all the best biomedical free web applications. Surf the website using the left sidebar and click on the star symbol. To insert here your favourite web applications. Physicochemical analysis of the primers. Protein structure and function prediction.

Lab conflict and how to address it. Conflict is a fact of life. Scientists should find ways to manage it in the lab, says Benjamin Tsang. The closing date is 5 April 2018.

Username is your email address. Answer to Password Retrieval Question. Increased coverage of RefSeq transcripts. Added a CRAVAT single variant annotation page that can be linked to externally.

What is the DDD study? What is a genome? Technologies used in DDD. How we process your sample. Recruitment into the DDD study has now finished. We are analysing every child recruited to the study, including those where parental samples were not received, and updates will continue to be be posted here. The DDD Study is aiming to issue a report to the clinical teams on all participants by the end of 2017, but research on undiagnosed families will continue until at least 2021.

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News about the Ensembl Project and its genome browser. Google Summer of Code 2018. New data and web features. 2018 a year of conferences.

Extracting useful information from large genomic datasets. The MacArthur lab uses cutting-edge genomic technologies at massive scale to understand the impact of human genetic variation, and to provide answers to families affected by rare genetic diseases. We lead an international consortium that has assembled ExAC. Is an intuitive online portal for exploring exome and whole-genome sequencing data from rare disease families.

A database of mammalian mitochondrial localisation evidence, phenotypes and diseases. 0? An integrated web resource of mitochondrial localisation evidence and phenotype data for mammals, zebrafish and yeasts. MitoMiner is now gene centric. With all data attached to gene objects. If you are short of time, just navigate through our set of Feature Hints.

List of web servers and software programs. New version of medaka genomic resource by SMRT long read sequencing. Kazuki Ichikawa, Jun Yoshimura, Koichiro Doi,. Shingo Tomioka, Yuta Suzuki. Process SMRT sequencing kinetic summary to predict regional methylation on large genome. A simple but powerful heuristic method for accelerating k-means clustering of large-scale data in life science. Rapid detection of expanded short tandem repeats in personal genomics using hybrid sequencing.