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Massive Parallel Sequencing
Massive Parallel Sequencing, also called Next Generation Sequencing, describes high-throughput DNA sequencing methods. There are three general steps involved in Massive Parallel Sequencing: 1) DNA sequencing libraries are made by amplifying DNA, 2) DNA is sequenced, 3) amplified DNA templates are sequenced. The DNA is sequenced simultaneously and in parallel allowing high throughput genetic analysis.
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FEB 14, 2023 | 10:00 AM
Date: February 14, 2023 Time: 10:00am (PST), 1:00pm (EST), 7:00pm (CET) The dorsal pontine tegmentum (PnTg) is part of the Pons, the largest section of the brainstem. It is a complex region...APR 20, 2022 | 5:30 AM
Esophageal adenocarcinoma [EAC] is the fastest growing in incidence cancer in the US over the last 25 years, while also having a 5 year survival of less than 20%. Barrett’s Esophagus [...JAN 31, 2022 | 6:00 AM
Date: January 31, 2022 Time: 6:00am (PST), 9:00am (EST) The advent of massively parallel next‐generation DNA sequencing (NGS) technologies has provided opportunities to radically improve str...OCT 14, 2021 | 7:00 AM
Date: October 14, 2021 Time: 7:00am (PDT), 10:00am (EDT) Heterologous protein expression in model organisms has many applications, including protein engineering, production of industrial enz...AUG 25, 2021 | 8:00 AM
Date: August 25, 2021 Time: 8:00am (PDT), 11:00am (EDT) Heterologous protein production is an indispensable tool in biotechnology and biopharma for manufacturing enzymes, protein therapeutic...APR 14, 2021 | 1:30 PM
Several SARS-CoV-2 variants are circulating globally. The most prominent variants of concern, including the B.1.1.7, B.1.351 and B1.1.28 lineages, not only carry a constellation of genetic m...Speaker: Anthony Tong, PhD , Subodh NimkarSEP 30, 2020 | 9:00 AM
While transformative, first-generation CRISPR technologies remain limited across multiple important dimensions including scalability, editing efficiency, types of modifications available, an...Speaker: Nandini Krishnamurthy, PhDJUL 16, 2020 | 10:00 AM
DATE: July 16, 2020 TIME: 10:00 am PDT This seminar reviews clinical utility of adopting rapid IDH1/2 testing in both hematological and solid tumors and describes the adjusted workflow devel...MAY 06, 2020 | 12:00 AM
The current standard methodology in forensic DNA typing relies on amplification of short tandem repeat (STR) markers by the polymerase chain reaction (PCR) and allele sizes (i.e., length-bas...MAY 06, 2020 | 12:00 AM
Learning Objectives: 1. Molecular basis of microhaplotypes 2. Informativeness and power of discrimination of microhaplotypes 3. Mixture deconvolution via microhaplotypes...APR 23, 2020 | 7:30 AM
The development of automated DNA sequencers using fluorescent di-deoxy nucleotide sequencing and capillary electrophoresis made it possible to generate the first draft sequences of the human...APR 02, 2020 | 2:30 PM
BGI group has been at the forefront in the fight against covid-19. Starting from building a lab in Wuhan, sequencing first 2019-nCoV virus genome and offering RT-PCR and sequencing based det...Speaker: Subodh Nimkar , Pan Zhang, PhDJUN 20, 2019 | 10:30 AM
The development of automated DNA sequencers utilizing Sanger sequencing and capillary electrophoresis made it possible to develop the first draft sequences of the human genome. The cost of do...JUN 21, 2018 | 12:00 PM
Advances in DNA sequencing, based upon massively parallel sequencing, has resulted in dramatic advances in DNA sequence output in the past few years. It is now possible to generate terrabases...MAY 11, 2017 | 10:30 AMC.E. CREDITS
Nucleotide variation in gene regulatory elements is a major cause of human disease. Despite continual progress in the cataloging of these elements, little is known about the code and grammati...MAY 11, 2017 | 7:30 AMC.E. CREDITS
Genetic testing currently plays a relatively niche role in healthcare, with testing typically limited to single genes and targeting a relatively narrow range of diseases, including paediatric...MAY 10, 2017 | 6:00 AMC.E. CREDITS
Massive parallel sequencing (MPS) technologies have paved the way into new areas of research including individualized medicine. However, sequencing of trace amounts of nucleic acids still rem...Speaker: Andrey Turchinovich, PhDMAY 13, 2015 | 9:00 AM
A well done RNA-Seq experiment can provide the most comprehensive, accurate and unbiased way to study gene expression, alternative splicing, RNA variation and RNA structure. The past few yea...AUG 22, 2013 | 10:00 AMC.E. CREDITS
The advent of massively parallel sequencing by next generation sequencing platforms now allow genomic approaches for individualizing healthcare. Genomic sequencing data reveals variants in ge...AUG 21, 2013 | 10:00 AMC.E. CREDITS
Massively parallel sequencing technology has proven to enable the identification of driver genetic alterations in patients' tumors that may be suppressed by targeted therapies. Through retros...
FEB 14, 2023 | 10:00 AM
Date: February 14, 2023 Time: 10:00am (PST), 1:00pm (EST), 7:00pm (CET) The dorsal pontine tegmentum (PnTg) is part of the Pons, the largest section of the brainstem. It is a complex region...
APR 20, 2022 | 5:30 AM
Esophageal adenocarcinoma [EAC] is the fastest growing in incidence cancer in the US over the last 25 years, while also having a 5 year survival of less than 20%. Barrett’s Esophagus [...
JAN 31, 2022 | 6:00 AM
Date: January 31, 2022 Time: 6:00am (PST), 9:00am (EST) The advent of massively parallel next‐generation DNA sequencing (NGS) technologies has provided opportunities to radically improve str...
OCT 14, 2021 | 7:00 AM
Date: October 14, 2021 Time: 7:00am (PDT), 10:00am (EDT) Heterologous protein expression in model organisms has many applications, including protein engineering, production of industrial enz...
AUG 25, 2021 | 8:00 AM
Date: August 25, 2021 Time: 8:00am (PDT), 11:00am (EDT) Heterologous protein production is an indispensable tool in biotechnology and biopharma for manufacturing enzymes, protein therapeutic...
APR 14, 2021 | 1:30 PM
Several SARS-CoV-2 variants are circulating globally. The most prominent variants of concern, including the B.1.1.7, B.1.351 and B1.1.28 lineages, not only carry a constellation of genetic m...
Speaker:
Anthony Tong, PhD
, Subodh Nimkar
SEP 30, 2020 | 9:00 AM
While transformative, first-generation CRISPR technologies remain limited across multiple important dimensions including scalability, editing efficiency, types of modifications available, an...
Speaker:
Nandini Krishnamurthy, PhD
JUL 16, 2020 | 10:00 AM
DATE: July 16, 2020 TIME: 10:00 am PDT This seminar reviews clinical utility of adopting rapid IDH1/2 testing in both hematological and solid tumors and describes the adjusted workflow devel...
MAY 06, 2020 | 12:00 AM
The current standard methodology in forensic DNA typing relies on amplification of short tandem repeat (STR) markers by the polymerase chain reaction (PCR) and allele sizes (i.e., length-bas...
MAY 06, 2020 | 12:00 AM
Learning Objectives: 1. Molecular basis of microhaplotypes 2. Informativeness and power of discrimination of microhaplotypes 3. Mixture deconvolution via microhaplotypes...
APR 23, 2020 | 7:30 AM
The development of automated DNA sequencers using fluorescent di-deoxy nucleotide sequencing and capillary electrophoresis made it possible to generate the first draft sequences of the human...
APR 02, 2020 | 2:30 PM
BGI group has been at the forefront in the fight against covid-19. Starting from building a lab in Wuhan, sequencing first 2019-nCoV virus genome and offering RT-PCR and sequencing based det...
Speaker:
Subodh Nimkar
, Pan Zhang, PhD
JUN 20, 2019 | 10:30 AM
The development of automated DNA sequencers utilizing Sanger sequencing and capillary electrophoresis made it possible to develop the first draft sequences of the human genome. The cost of do...
JUN 21, 2018 | 12:00 PM
Advances in DNA sequencing, based upon massively parallel sequencing, has resulted in dramatic advances in DNA sequence output in the past few years. It is now possible to generate terrabases...
MAY 11, 2017 | 10:30 AM
C.E. CREDITS
Nucleotide variation in gene regulatory elements is a major cause of human disease. Despite continual progress in the cataloging of these elements, little is known about the code and grammati...
MAY 11, 2017 | 7:30 AM
C.E. CREDITS
Genetic testing currently plays a relatively niche role in healthcare, with testing typically limited to single genes and targeting a relatively narrow range of diseases, including paediatric...
MAY 10, 2017 | 6:00 AM
C.E. CREDITS
Massive parallel sequencing (MPS) technologies have paved the way into new areas of research including individualized medicine. However, sequencing of trace amounts of nucleic acids still rem...
Speaker:
Andrey Turchinovich, PhD
MAY 13, 2015 | 9:00 AM
A well done RNA-Seq experiment can provide the most comprehensive, accurate and unbiased way to study gene expression, alternative splicing, RNA variation and RNA structure. The past few yea...
AUG 22, 2013 | 10:00 AM
C.E. CREDITS
The advent of massively parallel sequencing by next generation sequencing platforms now allow genomic approaches for individualizing healthcare. Genomic sequencing data reveals variants in ge...
AUG 21, 2013 | 10:00 AM
C.E. CREDITS
Massively parallel sequencing technology has proven to enable the identification of driver genetic alterations in patients' tumors that may be suppressed by targeted therapies. Through retros...