Exome Alignment Software


Lasergene Genomics Suite


DNASTAR's Lasergene Genomics Suite allows users to effortlessly align exome data against a genomic reference sequence and perform comprehensive post-alignment analysis, including identifying SNPs and structural variants, and reviewing coverage. Features of the Lasergene Genomics Suite software include:


  • Support for both single-end and paired-end data
  • The ability to align multiplexed data or multiple samples simultaneously
  • Large-scale SNP comparisons across individuals and groups
  • Advanced gene filtering based on the level of disruption to each gene caused by variations
  • Support for all major sequencing technologies


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PDF Icon Rapid Assembly and Analysis of Clinical Sequencing Data on a Desktop Computer: Using DNASTAR Software to Identify Potential Disease-Causing Mutations



Lasergene Genomics Suite Exome Alignment Benchmarks
Data Set Sequence
Technology
Reference
Sequence
Genome
Size (Mbp)
Number of
Reads (M)
Number of
Bases (Mbp)
Read
Length (bp)
Coverage Assembly
Time**
8 Human Exomes* (multiplex) Illumina Hg19+dbSNP 27 1,268 12,047 76 446X 14 Hrs
Human Exome* Illumina Hg19+dbSNP 27 163 12,390 76 459X 2 Hrs.

*Data sets for these projects were obtained from NCBI's Short Read Archive.
** Assembly times were calculated using a computer with a 4 Disk RAID-0.

Next-Gen Software
For All Major Sequencing Technologies