A Core-tailored Platform for Pinpointing Clinically Relevant Variants in Human Genomes and Exomes

Genomic studies of human disease and drug response aim to find one or a few causal variants among millions of possible candidates. A streamlined platform for quickly and reliably assessing each variant called in such studies can save months of tedious effort, speeding discoveries for core labs'...

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Hlavní autoři: Richards, D., Flannery, R., Kramer, A., Kutchma, A., Lerman, J., Leschly, J., Majumdar, S., Marshall, N., Molloy, M., Muthiah, A., Ning, A., O'Connor, R., Patel, K., Rajaraman, V., Rebres, R., Sarver, A., Su, H., Zhou, W., Zhu, X., Bassett, D., Pearson, Nathan
Médium: Artigo
Jazyk:Inglês
Vydáno: Association of Biomolecular Resource Facilities 2013
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Poster Session Abstracts
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3635303/
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