An Integrated Solution for De Novo Transcriptome Analysis
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Protected: Improving Genome Assemblies with PacBio HiFi Sequencing
There is no excerpt because this is a protected post.
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DNASTAR Celebrates 40 Years of Innovation
Computers have made steady advancement over the past 40 years and so has our...
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Phased Variant (Haplotype) Analysis for Whole Genome Sequencing
Lasergene 18 enables end- to-end assembly and analysis of long-read sequencing data from human...
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How to Assemble Genomes like a Bioinformatics Pro
Whether you are working with Illumina, Oxford Nanopore, PacBio data, or a combination of...
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Using Lasergene to De Novo Assemble PacBio HiFi Data
Learn more about PacBio HiFi sequencing, a hybrid of short- and long-read sequencing that...
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Q&A: Assembling and Analyzing NGS & Long Read Sequences
This post answers some recent DNASTAR customer questions related to NGS and long read...
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Free NGS Assembly and Alignment in the Cloud
Whether you've licensed Lasergene or want to do a free trial, you automatically get...
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7 Tips for Learning New Genomics Software
You’ve prepped your samples, submitted them for sequencing, and finally received a file with...
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Variant Annotation with Lasergene Genomics: The easy way to discover, annotate and filter sequence variants
Once you find thousands of variants in a set of samples, how can you...
