Bioinformatics and Genomics Gateway
Welcome to the BioMed Central Bioinformatics and Genomics gateway, highlighting the latest news and information from BioMed Central and from across the web, on Bioinformatics and Genomics.
An analysis of HER2 heterogeneous breast cancers reveals an important role of the HER2 negative component of the HER2 positive tumors
Abnormal RNA splicing is a common characteristic of cancers and suggests that intron-containing mRNAs contribute to the transcriptional diversity of many cancers
Partial protein domains are characterized, and are found to be largely alignment or annotation artifacts
Do women with eating disorders who have social and flexibility difficulties really have autism? This case series raises the alarm in relation to potential under-/misdiagnosis or diagnostic 'overshadowing' in females with autism.
HaploShare is a method for identification of extended haplotypes shared by cases and for comparison against controls
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Previously published by Henry Stewart Publications, Human Genomics has now launched and is accepting submissions under BioMed Central's open access platform. Edited by Prof. Vasilis Vasiliou, the journal aims to facilitate rapid publication and stimulate discussion within the human genomic field. The journal welcomes manuscripts relating to the application of genomic analysis in the understanding, treatment and diagnosis of complex and Mendelian diseases, as well as reports of the genomic analysis of adverse drug reactions, drug efficacy and safety.
BMC Medical Informatics and Decision Making 2015, 15(Suppl 1):S7
BMC Genomics 2015, 16:388
BMC Cancer 2015, 15:407