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: SWEGEN
Submitter Method ID: ILLUMINA_WGS
Submitted method description:
Human whole genome sequencing on the Illumina system at an average coverage of 30X per sample
PARAMETER:
Input: 1 µg genomic DNA extracted from human blood samples
Library preparation: TruSeq DNA PCRfree sample preparation kit
Sequencing: Paired-end 150bp sequencing on Illumina HiSeqX

This method was used in the following submission:

Submitter Handle Batch Type Submitter batch id Release build id
SWEGEN Assay SWEGEN 150