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PacBio single molecule real time (SMRT) applications - Webinars

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PacBio single molecule real time (SMRT) application - Webinars & Tutorials


PacBio third generation sequencing technology applications - Webinars 

Highlighting Unexplored Genomic Regions with SMRT Sequencing: Informatics for Structural Event Detection in PacBio

This webinar explains the advantage for long read application in repetitive region, in detection and sequencing of structural variants (SV) including insertions and deletions.

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High-throughput NGS for Screening of Microbial Pathogens

This webinar introduces a workflow for sequencing of bacteria with PacBio technology in 2-3 days. The application of the PacBio technology for virus sequencing is demonstrated by an example of the cervial cancer causing papillioma virus (HPV). It is stated that the NGS technology is much more sensitive as any other method for HPV detection. NGS is discussed in the context of the detection of new virus strain.

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No Assembly Required: Extremely Long Reads for Full-length Transcript Isoform Sequencing

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Patterns of Structural Rearrangement in Cancer Revealed by Ultra-Long Read Sequencing

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Resolving Complexity of the Human Genome

(33 min, 2014) The webinar describes the benefits of using the PacBio technology for resequencing of human genomes. The long read technology enables the closing of gabs in the human genome that is not possible with other NGS technologies based on short reads. These gabs are especially found at the end of the chromosomes and the technology is suitable for telomere sequencing. The PacBio technology enables the detection of new structural variants including insertions, deletions, and inversion duplications. It was argued that the cost for one human genome with this technology is about 50-80000 dollar.

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Sequencing the Unsequenceable: Expanded CGG-repeat Alleles of the Human FMR1 Gene

(20 min, 2012) The webinar discusses the problem of sequencing CGG repeats caused by mutation. High number of CGG repeats (+200) cannot easily be sequenced with short read based NGS technologies. Additional, the sequencing and detection of CpG methylation sides in these repetitive regions is discussed.

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Simplified Characterizations of Large Deletions using the PacBio Sequencing Platform

This webinar discusses the advantages of large deletions detection using PacBio technology compared to conventional PCR and Sanger sequencing.

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Targeting Complex Structural Motifs in Genes and Haplotypes with Long-Read SMRT® Sequencing

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Validation and replication for human resequencing projects

This webinar discuss the application and advantage of the PacBio technology for resequencing of human genome regions. It describes the results of an comparison study for SNP calls with the PacBio and the Illumina technology.

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Whole human genome SMRT sequencing reveals uncharacterized variations providing a path to more informed diagnostic testing

(21min, 2013) The advantage of the PacBio technology is described for the detection and sequencing of repeats in the human genome.

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