NEB® at AGBT™ 2019
We’re looking forward to seeing you at AGBT! We are proud to be a Bronze Sponsor again and have a lot of exciting NEBNext® updates to share with you.
Hear more about the latest technologies
BRONZE SPONSOR WORKSHOP
Advances in Genome-wide Methylation Profiling
Jennifer Ishii, Sequencing Development Manager, The New York Genome Center
Friday, March 1st, 2:35 – 2:55 PM
POSTER FLASH TALK
ReCappable-seq and Nanopore ReCappable-seq: Comprehensive Determination of pol I, pol II and pol III Transcription Start Sites and Full Length Transcripts in Eukaryotes
Laurence Ettwiller, New England Biolabs, Inc, Ipswich, MA
Thursday, February 28th 11:30 – 11:50 AM
Suite presentations:
Deciphering the Methylome: Enzymatic Methyl-seq
Louise Williams, Ph.D. and Chaithanya Ponnaluri, Ph.D.
Thursday, February 28th 8:00 – 8:30 AM
Saturday, March 2nd 8:00 – 8:30 AM
Shifting the Paradigm for Targeted Re-sequencing: NEBNext Direct® Custom Ready Panels
Andrew Barry, M.S.
Friday, March 1st 8:00 – 8:30 AM
Learn what's new and coming soon from NEBNext
Visit posters in our suite, and meet our scientists to learn about topics including:
An enzymatic alternative to bisulfite sequencing with superior performance
COMING SOON: The NEBNext Enzymatic Methyl-seq Kit (EM-seq™) provides an enzymatic alternative to whole genome bisulfite sequencing (WGBS),
combined with high-efficiency, streamlined library preparation.
- Superior sensitivity of detection of 5-mC and 5-hmC
- Larger library insert sizes
- More uniform GC coverage
- Greater mapping efficiency
RNA Depletion
COMING SOON: New options for depletion of abundant RNAs, including globin and bacterial samples, and a custom solution.
NEBNext Direct Custom Ready Panels
Customize your focused enrichment panel and receive a sequence verified panel in two weeks. Choose from our list of 850 genes.
NEBNext Ultra™ II FS DNA Library Prep
Novel enzymatic fragmentation integrated seamlessly into the library prep workflow.
NEBNext Single Cell/Low Input RNA Library Prep
Uniform full-length transcript coverage; unmatched detection of low abundance transcripts.
Visit our conference posters
| Poster Title | Authors |
|---|---|
| Selective Removal of Abundant RNAs and Use of Unique Molecular Identifiers Increases Transcriptome Profiling Sensitivity in Eukaryote and Blood Samples | Deyra Rodriguez, New England Biolabs, Inc, Ipswich, MA |
| RADAR-seq: a RAre DAmage and Repair Sequencing Method for Detecting, Locating and Quantifying Physiological Levels of DNA Damage on a Genomewide Scale | Vladimir Potapov, New England Biolabs, Inc, Ipswich, MA |
| Also a Featured Poster Talk, February 28th, 11:30 – 11:50 AM ReCappable-seq and Nanopore ReCappable-seq: Comprehensive Determination of pol I, pol II and pol III Transcription Start Sites and Full Length Transcripts in Eukaryotes |
Laurence Ettwiller, New England Biolabs, Inc, Ipswich, MA |
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