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Strand
- Strand is now a friend with Seema Singh
- Strand published a news post Webinar on Diagnosis of Rare Diseases using NGS Based Multi-gene Testing- Case studies by Dr.Aparna...Comments
- Strand 2881 days ago
Hurry! Limited seats available. Register to attend here http://www.strand-ngs.com/webinar_registration
- Strand 2872 days ago
Those who missed the webinar, could watch the recording here http://www.strand-ngs.com/sites/default/files/private/videos/webinars/rare-disease-diagnosis.mp4
- Strand created a page Webinar on RNA-Seq Data Analysis on 28 Feb 2018
- Strand is now a friend with Radha Agarkar
Live Webinar on RNA-Seq Data Analysis on 9 Nov 2016
By Strand 3425 days agoLive Webinar on RNA-Seq Data Analysis Abstract: Strand NGS supports an extensive workflow for the analysis and visualization of RNA-Seq data. The workflow includes Transcriptome / Genome alignment, Differential expression analysis with Statistical...Webinar on Implications of Next Generation Sequencing in Molecular Diagnosis of Cancer on 28 Sep...
By Strand 3473 days agoLive webinar on Implications of NGS in molecular diagnosis of cancerCalling narrow and broad peaks from ChIP-Seq data
By Strand 3867 days agoCalling narrow and broad peaks from ChIP-Seq dataIntegrated mRNA and microRNA transcriptome analysis in Strand NGS
By Strand 3867 days agoIntegrated mRNA and microRNA transcriptome analysis in Strand NGS
Webinar on RNA-Seq Data Analysis on 28 Feb 2018
Last updated 2934 days ago by StrandStrand NGS is a biologist friendly NGS analysis tool that allows biologists to analyze their data using a very intuitive workflow for the analysis and visualization of RNA-Seq data. This webinar will give an overview of the workflow which includes...
Webinar on Diagnosis of Rare Diseases using NGS Based Multi-gene Testing- Case studies by Dr.Aparna...
By Strand 2909 days ago Comments (2)A disease is considered to be ‘rare’ when it affects one in about 2000 individuals in the population. This, individually are although rare, collectively, the incidence could be very high causing a significant socio-economic burden....Webinar: Unravelling complex mutational events in clinical cases using the power of NGS data...
By Strand 2992 days agoNGS webinarJoint webinar by Agilent Technologies and Strand Life Sciences on 'Analysis of Variants using...
By Strand 3033 days agoAgilent, Strand, variant analysis, GenespringWebinar on Unique Molecular Identifier (UMI)-powered Ultra-sensitive Variant Calling using Strand...
By Strand 3041 days ago Comments (1)Webinar on Unique Molecular Identifier-powered Ultra-sensitive Variant Calling using Strand NGS - Case Study by Dr. Pandurang Kolekar, Bioinformatics Engineer, Strand Life Sciences Abstract: Unique Molecular Identifiers (UMIs) are short...
Jit
5557 points
5557 points
Jitendra Narayan
2550 points
2550 points
Rahul Nayak
2300 points
2300 points
Neel
1639 points
1639 points
BioStar
1266 points
1266 points
Question: Any good bioinformatics suggestions !
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Question: Alienomics error, how to fix it !
Question: What is the p-value?
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