DNA Sequence Extraction

  Reference Genome:
  Coordinate: 1-based 0-based
  Strand:  both forward reverse

For Genomic Variants in VCF
  Window Size: (in bp)
uniform (+/-):   bp
different   (+):   bp (-):   bp
  Nearest Splice Site Annotation: no canonical all
  Neighbor Variants Within Window: no yes
  Output Sequence:   ref & alt ref alt
    Genomic Variants: (no more than 10,000 genomic variants)
   provide the first 5 columns of the genomic variants in VCF format. (check sample VCF)

   or, upload the genomic variants in VCF file:


For Genomic Ranges in BED
   Genomic Ranges: (no more than 10,000 genomic ranges)
   provide the first 3 columns of the genomic ranges in BED format. (check sample BED)

   or, upload the genomic ranges in BED file:


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