2023 Poster Abstracts - Please click the links below for access

A comparison of ambient RNA and gene detection between split pool combinatorial barcoding and droplet-based technologies

A Customized Approach to Spatial Transcriptomics and Proteomics

A microfluidics-free approach for simultaneously profiling the whole transcriptome and TCR repertoire of 1 million cells in a single experiment

A Model Comparability Study between C1000 Touch Thermal Cyclers and PTC Tempo Thermal Cyclers

A Novel Method For Generating Unprecedented Ultra-High-Sequence Diversity Libraries Of Plasmids And Recombinant Viruses (With Validation) For High-Throughput Screening, drug discovery And Targeted Therapy

A Novel Next-Gen Sequencing Library Preparation Method To Sequence Small, Long, And Low-Quality (Fragmented/ Degraded) RNA With low Quantity Of Templates (pico-grams) For improved Diagnostics, Biomarker Discovery, And Research

A novel suite of enzyme mixes enable robust hybrid capture sequencing from low quality FFPE DNA

A novel, streamlined workflow for high-throughput whole transcriptome RNAseq library preparation

A rapid, automated whole transcriptome library preparation solution to support a variety of applications and sample types

A robust search strategy for acknowledgments of core contributions in scientific publications

A soil microbial workflow from DNA extraction to amplicon sequencing

A Study in Matrix Interference: The Pierce Quantitative Fluorometric Peptide Assay and the SUMS Proteomics Landscape

ABRF DNA Sequencing Research Group, DSRG

Advanced microbiome tools for metagenomics

Advancements in microwell-based single-cell analysis technology allow high-throughput capture and pr

Analysis of Microsatellite Instability using the new SeqStudio Flex Capillary Electrophoresis Instrument

Assessment of cell type identification methods for single-cell and spatial transcriptomic analysis in mouse

Automated DNA Cleanup for NGS Workflow

Automating Low-Throughput Library Prep Workflows for Core Facilities

Automating NEBNext® Enzymatic Methyl-seq Kit Using the Biomek i7 Hybrid NGS Workstation for Whole Genome Methylation sequencing

Baylor College of Medicine Biotechnology Research Incubator for Teachers

Biotechopoly: A Serious Science Game for Raising Career Interest

Building Customer Service-Oriented Integrated Cores for Molecular Research at UTHSC

Cloudbreak Chemistry from Element Biosciences: Higher accuracy, shorter run times, simplified workflow

Cold Spring Harbor Laboratory Functional Genomics Facility

Collaborative Data Management and Sharing: Cores in Partnership with FASEB DataWorks!

Community-driven FAIR data management and reproducibility for the entire imagedata life cycle

Comparative Analysis of RNA-Seq Library Prep Kits for Shared Research Resource Facilities

Comparative Assessment of Low Input ChIP-seq Library Kits

Comparing the NextSeq 2000 to the MiSeq sequencer for amplicon-based reads

Comparison of DNA and RNA Assays Using Agilent Automated Electrophoresis Systems

Degradome re-annotation of single-cell RNAseq datasets identifies signatures of miRNA biogenesis and apoptosis

Determining the interaction site of a novel Coprinopsis cinerea lectin to Listera innocua peptidoglycan

Developing 3D printing solutions and improvements for flow cytometry

Development of a novel, probe-based and instrument-free method for ultrahigh-throughput single-cell gene expression analysis, TempO-LINC

Development of a Sequencing Core with Embedded Bioinformatics to Address High-throughput Sequencing Concerns

Development of control peptides for immunoaffinity-based enrichment of posttranslationally modified peptides

Development of custom morphology markers for NanoString GeoMx Digital Spatial Profiler enables better tissue stratification to study tumor heterogeneity

Effects of particle size on drop delay accuracy and subsequent recovery in cell sorting; a multi-institutional, multi-sorter study

Efficient and sensitive high-throughput mouse immune repertoire profiling using SMART technology

Efficient Workflows for Electron Microscopy Laboratories by Using Automated Specimen Preparation

Electron Microscopy Core Imaging Facility: Imaging Shared Service

Enabling Access to Biomolecular Crystallization Capabilities with Robotics and Advanced Imaging

EPIGENOMICS SHARED FACILITY (ESF)-EXPANDING ANNOVATIVE CAPABILITIES

Exploring the veterans’s pipeline

Extended capability of Visium CytAssist to enable highly-sensitive transcriptomic profiling of PFA fixed, OCT embedded biological specimens

FAIR Facilities and Instruments: Standardization and Adoption of Persistent Identifiers (PIDs) for Research Facilities and Instruments

Financial Dashboard

Flow Cytometry Research Group

Flow Cytometry Shared Resource at the Sylvester Comprehensive Cancer Center

Functional Imaging of Optical Electrophysiology is getting ready for Pre-/Clinical Applications

Genome Technology Core at Whitehead Institute

Genomic Sequencing and Analysis with Aviti in a High-Throughput, Multi-user Environment: Introducing AvitiOS 2.0 and Elembio Cloud

Gloucester Biotechnology Academy: An Innovative Pathway to Laboratory Careers

High compatibility for RNA sequencing using the Element AVITI™ System and the Bio-Rad SEQuoia™ Express and SEQuoia™ Complete Stranded RNA Library Prep Kits

High-Throughput Single Cell Sequencing on the G4™ Using the Novel Max Read™ Kit

Hybrid open-top light-sheet microscopy for high throughput 3D imaging of cleared tissues

Implementation and Management of MERFISH Spatial Transcriptomics in the SCOPE Core Facility

Implementation and Project Management Workflow of the GeoMx Digital Spatial Profiling Platform in the SCOPE Imaging Core Facility

Improved RNA stability and integrity for better RNAseq data

Increasing observability of the phosphoproteome in brain tissue

Intraoperative Collection of Neurosurgical Biorepository Tissue

Levitation Technology for Unperturbed Cell Isolation

Mapping the spatial heterogeneity of the tumor microenvironment by hyperplex immunofluorescence with COMET™

Maxwell® Genomic DNA Kit: A broad sample type genomic DNA extraction kit

Method comparison for circulating free fetal DNA (cffDNA) extraction from plasma samples of women during pregnancy in support of noninvasive perinatal sequencing for precision medicine prenatal care

Methods for improved throughput and quality in long-read RNA sequencing workflows

NEBNext UltraShear™: Novel Enzymatic Fragmentation for Challenging Samples and Methods

Novel high-throughput single cell analytical methods using Particle-templated Instant Partitions (PIPseq™)

Opening a New Door into Biotechnology Careers: Development of a Core Technology Scholars Program

Optimizing single nuclei sequencing of brain samples from spaceflown mice across age and strain

Overcoming Limitations of RNA-Seq Library Construction from FFPE Samples Using a Novel Workflow

Performance evaluation of the G4 sequencing platform for microbiome community analysis

Preventing Sample Bias in scRNAseq introduced by Cryopreservation: A Solid Tumor Case Study

REPORTING OF MICROSCOPY METADATA – HOW TO IMPROVE QUALITY AND REPRODUCIBILITY IN BIOIMAGING

Rigor, Reproducibility, and Transparency in Shared Research Resources: Follow-Up Survey and Recommendations for Improvements

Robust, Streamlined, Express DNA Library Preparation Methods Meet Requirements of High-throughput Library Construction

Scalable and Flexible Single Cell RNA-seq

Scaling Up and Out: Data and Informatic Architectures to Meet High Volumes of Diverse Sequencing Applications

Showcasing the functional profile of murine fecal samples using whole metagenomic and metatranscriptomic data together

Simultaneous profiling of RNA and chromatin accessibility by multiomic Assay for Transposase-Accessible Chromatin with sequencing (ATAC-Seq) using microwell-based single-cell partitioning technology

Single Cell Sequencing Using the Parse Biosciences Evercode™ WT Kit on the G4™ Sequencing Platform

Smart Deep Basecaller, AI-based Basecaller for Sanger Sequencing

SYNTAX system enables rapid probe synthesis and testing to accelerate custom qPCR assay development

The role of Shared Resources in facilitating human and environmental surveillance for SARS-CoV-2

The Singular Genomics G4 Sequencing Platform offers rapid, cost-effective RNA sequencing (RNA-Seq) with four flow cell flexibility and single-day run times

Total Nucleic Acids Extraction from FFPE Samples using Adaptive Focused Acoustics® (AFA®) Technology for Comprehensive Genomic Profiling

Universal mouse reference RNA as a standard metric for evaluating bulk RNA-seq data

Use of isotachophoresis for successful nucleic acid extraction from difficult specimens in the Biospecimen Processing Core Facility at the University of North Carolina at Chapel Hill

Using PowerBI to create and effectively communicate Core metrics and equipment roadmaps

Vanderbilt Cell Imaging Shared Resource

Vermont Biomedical Research Network Cores

Visualizing DNA for Long Read Sequencing by Moles, not Mass

Whole genome sequencing with increased insert length eliminates over 25% of errors in challenging medically relevant genes

Whole transcriptome spatial profiling of fresh frozen tissue samples using two RNA-capture methods