NCBI
dbSNP

dbVar ClinVar GaP PubMed Nucleotide Protein
Search small variations in dbSNP or large structural variations in dbVar
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Method Detail
Submitter Method Handle: JJLAB
Submitter Method ID: ILLUMINA HISEQ X TEN WHOLE GENOME SEQEUNCING
Submitted method description:
Sequencing library preparation was carried out according to Illumina HiSeq X Ten protocol. 150 basepairs paired end reads were obtained from HiSeq X Ten sequencer. Reads alignment was conducted with Burrows-Wheeler Aligner and SNP calling by Genome Analys

This method was used in the following submission:

Submitter Handle Batch Type Submitter batch id Release build id
JJLAB Assay WHOLE GENOME SNPS DISCOVERY 147
JJLAB Assay WHOLE GENOME INDELS DISCOVERY 147