ABRF 2022
Sunday, March 27 – Wednesday, March 30
Palm Springs Convention Center
Join PacBio at ABRF 2022 to learn more about how service providers worldwide are adding PacBio Systems to their portfolios to meet the growing demand for HiFi sequencing.
Below you’ll discover the many ways to engage with us at the conference. We look forward to meeting you.
Not able to attend ABRF 2022? Fill out the form to receive our talk recordings and other materials we'll present at the conference.
Here are a few ways to engage with PacBio at this year's meeting:
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Tuesday, March 29, 7:30 am – 8:30 am
Smoketree C (Palm Springs Convention Center)
View Program
Staff Product Manager
PacBio
Associate Director, Product Marketing
PacBio
Michael Eberle, PhD, VP Computational Biology, PacBio
TBP
Tuesday, March 30, 9:30 am – 10:45 am
Speaker
Justin Blethrow, PhD
Staff Product Manager
PacBio
PacBio’s highly accurate long reads offer an unparalleled view of the genome, revealing all forms of variation from SNPs to large structural variants. HiFi reads also provide the best view of the transcriptome through full length sequencing of transcript isoforms. Now, HiFi sequencing also provides direct insight into the vertebrate epigenome and gene regulation through automatic calling of 5-methyl cytosine in native DNA.
Wednesday, March 30, 7:30 am – 8:30 am
Smoketree C (Palm Springs Convention Center)
Participating Speaker
Liz Tseng, PhD
Associate Director, Product Marketing
PacBio
Talk title: CRISPR-based depletion of ubiquitous or non-informative genes in bulk and single-cell full-length transcriptomes
Wednesday, March 30, 9:30 am – 10:45 am
Participating Speaker
Molly Zeller
Lab Manager
UWBC DNA Sequencing Facility
Talk title: It's PacBio sequencing time
Visit us at booth #305 to find out more
Official rules apply
# | Title | First Author | Date |
2046 | Automated repeat characterization of filaggrin from PacBio Sequel HiFi long reads | A. Hawes | February 28, 2022 |
2115 | Genomic variant detection within human segmental duplications | D. Soto | |
2123 | High-throughput sequencing and mapping technologies applied to 10 human genomes with chromothripsis-like rearrangements | U. Melo | |
2153 | Maximizing the quality of RefSeq annotation in the era of big data | S. Pujar | |
2189 | Profiling variable-number tandem repeat variation across populations using repeat-pangenome graphs on haplotype-resolved assemblies | T.-Y. Lu | |
2304 | Enlightening the dark matter of the genome: Whole genome imaging identifies a germline retrotransposon insertion in SMARCB1 in two siblings with atypical teratoid rhabdoid tumor | M. Sabatella | |
2335 | Genome-wide profiling of DNA methylation from a breast cancer and a matched normal cell lines | C. Xioa | |
2408 | Protective effect of 1p36.22 Ewing Sarcoma association locus is conferred by an allele specific GGAA-microsatellite duplication leading to TARDBP overexpression | S. Baulande | |
2444 | TrueXome technology is used for true gene enrichment and pseudogene suppression | P. Song | |
2906 | Identification of VNTR length polymorphism as a driver of local variation in DNA methylation levels | A. Martin | |
3024 | Telomere-to-telomere assembly and complete comparative sequence analysis of the human chromosome 8 centromere | G. A. Logsdon * | |
3207 | Long-read amplicon sequencing detects a bi-allelic SMN1 & SMN2 gene conversion allele that does not guarantee a spinal muscular atrophy (SMA) phenotype | D. Zeevi | |
3208 | Long-read sequencing and optical mapping decipher structural composition of ATXN10 repeat in kindred with spinocerebellar ataxia and Parkinson’s disease | B. Schuele | |
3287 | A new approach to Thalassemia and Ataxia carrier screening panels using CRISPR-Cas9 enrichment and long-read sequencing | Y. Tsai | |
3305 | Clinical application of long-read sequencing technology to neurodevelopmental disorder diagnosis | S. Hiatt * | |
3448 | Identifying novel structural variants at the 17q21.31 MAPT locus in progressive supranuclear palsy using targeted long-read sequencing | H. Walsh | |
3487 | Accurate, comprehensive variant calling in difficult-to-map genes using HiFi reads | W. Rowell * | |
3494 | Capture long-read isoform sequencing (Iso-Seq) for uncovering human isoform diversity in the brain and characterizing SARS-CoV2viral RNAs | T. Hon | |
3512 | Full-length transcript sequencing of human and mouse identifies widespread isoform diversity and alternative splicing in the brain | A. R. Jeffries | |
3520 | High molecular weight DNA extraction and long-read next-generation sequencing of human genomic reference standards | M. Mitchell | |
3523 | High-throughput HiFi library workflow for Human Whole Genome Sequencing on the Sequel II System | S. Chakraborty | |
3628 | Long read sequencing of the SARS-CoV-2 genome and the human immune repertoire | E. Tseng * |
# | Title | First Author | Date |
1062 | A high-resolution panel for uncovering repeat expansions that cause ataxias | Y. Tsai | Febraury 28, 2022 |
Stop by our booth to chat with PacBio staff, get all your questions answered, and see plant and animal genomics in action!
Book a meeting to talk to a PacBio scientist over a cup of coffee. We are excited to learn about your sequencing goals and learn more about your research!
Booth hours: