SNPFisher : Variant Report Compiler

Variation data for Additional Datasets compiled against reference Zv9

Variant frequency data from external data sources is merged against genetic backgrounds AB, TU, TL, and WIK

UCSC Format Ranges And/Or RefSeq Gene Names Batch Query : (UCSC format chrX:Y-Z ; Only One entry per line)
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(Your query may take a variable amount of time depending on filter settings and size of ranges selected)

Data presented comes from the following sources:

Bowen, M. E., Henke, K., Siegfried, K. R., Warman, M. L. and Harris, M. P. (2012). Efficient mapping and cloning of mutations in zebrafish by low-coverage whole-genome sequencing. Genetics 190, 1017-1024.

Obholzer, N., Swinburne, I. A., Schwab, E., Nechiporuk, A. V., Nicolson, T. and Megason, S. G. (2012). Rapid positional cloning of zebrafish mutations by linkage and homozygosity mapping using whole-genome sequencing. Development 139, 4280-4290.