Genome reference of GRCh38 is supported in Haplotype-based Variant Detection Analysis (30 Jan 2018).
Annotation of genomic variants are available in Low Frequency Variant Detection Analysis and RNA Variant Detection Analysis (28 Nov 2017).
Annotation of genomic variants is supported in Haplotype-based DNA Variant Detection Analysis (25 Sep 2017).
HiPipe provides high performance NGS
data analysis pipelines with intuitive user interface to the community
so that researchers with minimum IT or bioinformatics knowledge can
perform common analyses on NGS data. 3 TB of storage space is reserved
for each task. Please see Info for details.
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Genome & Exome Variant Detection
Pipelining raw sequences into BWA for
mapping and then into GATK for variant detection. Usually, a human
exome (100x) can be processed in one hour or so.