Join DNASTAR Senior Product Manager Matthew Keyser to learn how to quickly assemble large NGS data sets using a simple laptop or desktop computer, including a live demo of a multiple genome assembly and analysis.
ABOUT
March 21, 2019
11:00 AM CDT
At this webinar, you will learn to perform NGS sequence assembly and alignment for multiple genomes, exomes, and RNA-Seq samples from a desktop or laptop computer. Discover how to complete large projects with unmatched speed, even with limited hardware resources. With our new Cloud Assemblies option, multiple-sample assembly, variant calling, and normalization generally complete even faster than on the most powerful desktop computers.
ATTEND WEBINAR
Register on our website
Questions? Contact [email protected]
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by seqadmin
Amplicon sequencing is a targeted approach that allows researchers to investigate specific regions of the genome. This technique is routinely used in applications such as variant identification, clinical research, and infectious disease surveillance. The amplicon sequencing process begins by designing primers that flank the regions of interest. The DNA sequences are then amplified through PCR (typically multiplex PCR) to produce amplicons complementary to the targets. RNA targets...-
Channel: Articles
03-21-2023, 01:49 PM -
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by seqadmin
Targeted sequencing is an effective way to sequence and analyze specific genomic regions of interest. This method enables researchers to focus their efforts on their desired targets, as opposed to other methods like whole genome sequencing that involve the sequencing of total DNA. Utilizing targeted sequencing is an attractive option for many researchers because it is often faster, more cost-effective, and only generates applicable data. While there are many approaches...-
Channel: Articles
03-10-2023, 05:31 AM -
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