Excited to learn about prediction methods using statistical workflows? Register to the upcoming webinar by Dr Mario Deng, Professor of Medicine, UCLA and learn the application of NGS and Machine learning to predict post-operative recovery of advanced heart failure patients.
Details: 9 Aug 2017, 8 am PST. Register at http://www.strand-ngs.com/webinar_registration
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In case you missed the webinar, because of your busy schedule, you can access the recording here http://www.strand-ngs.com/learn/webinar-recordingsLeave a comment:
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Just a day to go for our webinar on DNA-Seq Data Analysis in StrandNGS. Hurry! Register at http://www.strand-ngs.com/webinar_registrationLeave a comment:
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Live webinar on DNA-Seq Data Analysis - Selected Case Studies on 22 Feb 2017
Webinar on DNA-Seq data analysis- Case Studies
DNA-Seq data can be analyzed and visualized using an extensive workflow in Strand NGS software. The software has been designed for the biologists. Strand NGS supports analysis of whole exome, whole genome and targeted sequencing experiments. The DNA-Seq workflow includes the ability to detect variants (SNPs, MNPs and short InDels), annotate them with dbSNP, and report for each SNP the kind of effect it has on the genes and provides list of affected genes. Biological contextualization of the affected genes can be performed by downstream analysis such as GO, GSA, pathway analysis.
Large structural variations, including large insertions, deletions, inversions, and translocations, can also be detected with paired-end and mate-paired data. Copy number variation (CNV) analysis can be done using tumor-normal pairs. Strand NGS has easy to use built in pipelines (with an option to customize) for time consuming jobs which automates analysis and leaves more time for end data interpretation. In this webinar we will discuss case studies using the DNA-Seq data analysis workflow in Strand NGS and also highlight on parameters within each feature that can be optimized depending on datasets and analysis needs.
Details:
Session 1: 2:30 PM IST, 22 Feb
Session 2: 10:30 PM IST, 22 Feb
Speaker: Dr. Suman Kapoor, Manager- Application Science at Strand Life Sciences, has over 10 years experience in molecular biology, next-generation sequencing based testing, clinical genomics, and personalized medicine for disease management and prenatal testing. Dr. Suman holds a Ph.D in Molecular and Cell Biology from Indian Institute of Science, Bangalore. Prior to joining Strand NGS team, Suman has worked extensively on protein synthesis in eubacteria and has experience working in CAP and NABL accredited lab validating and interpreting NGS based diagnostic tests.
Register here: http://www.strand-ngs.com/webinar_registration
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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...03-21-2023, 01:49 PM -
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...03-10-2023, 05:31 AM
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