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: LUNTER
Submitter Method ID: ILLUMINA_SHORT_SEQUENCE_DATA
Submitted method description:
DNA obtained from transformed B cell lines was sequenced using the Illumina Genome Analyzer
to low coverage as described in PMID:20981092, and the short reads obtained were used to call
indels across the human genome as described in the publication associated with this
submission.
PARAMETER: See PMID:20981092

This method was used in the following submission:

Submitter Handle Batch Type Submitter batch id Release build id
LUNTER Assay indel_calls_from_1000_genomes_pilot_1_CEU 136
LUNTER Assay indel_calls_from_1000_genomes_pilot_1_YRI 136
LUNTER Assay indel_calls_from_1000_genomes_pilot_1_JPTCHB 136