CRISPR screening in hematology research: from bulk to single-cell level

S Meyers, S Demeyer, J Cools - Journal of Hematology & Oncology, 2023 - Springer
The CRISPR genome editing technology has revolutionized the way gene function is
studied. Genome editing can be achieved in single genes or for thousands of genes …

Multiplexing methods for simultaneous large‐scale transcriptomic profiling of samples at single‐cell resolution

J Cheng, J Liao, X Shao, X Lu, X Fan - Advanced Science, 2021 - Wiley Online Library
Barcoding technology has greatly improved the throughput of cells and genes detected in
single‐cell RNA sequencing (scRNA‐seq) studies. Recently, increasing studies have paid …

Targeted Perturb-seq enables genome-scale genetic screens in single cells

D Schraivogel, AR Gschwind, JH Milbank, DR Leonce… - Nature …, 2020 - nature.com
The transcriptome contains rich information on molecular, cellular and organismal
phenotypes. However, experimental and statistical limitations constrain sensitivity and …

Prime-seq, efficient and powerful bulk RNA sequencing

A Janjic, LE Wange, JW Bagnoli, J Geuder, P Nguyen… - Genome biology, 2022 - Springer
Cost-efficient library generation by early barcoding has been central in propelling single-cell
RNA sequencing. Here, we optimize and validate prime-seq, an early barcoding bulk RNA …

Sample-multiplexing approaches for single-cell sequencing

Y Zhang, S Xu, Z Wen, J Gao, S Li… - Cellular and Molecular …, 2022 - Springer
Single-cell sequencing is widely used in biological and medical studies. However, its
application with multiple samples is hindered by inefficient sample processing, high …

New approach methodologies to facilitate and improve the hazard assessment of non-genotoxic carcinogens—a PARC project

M Audebert, AS Assmann, A Azqueta, P Babica… - Frontiers in …, 2023 - frontiersin.org
Carcinogenic chemicals, or their metabolites, can be classified as genotoxic or non-
genotoxic carcinogens (NGTxCs). Genotoxic compounds induce DNA damage, which can …

HyPR-seq: single-cell quantification of chosen RNAs via hybridization and sequencing of DNA probes

JL Marshall, BR Doughty… - Proceedings of the …, 2020 - National Acad Sciences
Single-cell quantification of RNAs is important for understanding cellular heterogeneity and
gene regulation, yet current approaches suffer from low sensitivity for individual transcripts …

scPNMF: sparse gene encoding of single cells to facilitate gene selection for targeted gene profiling

D Song, K Li, Z Hemminger, R Wollman, JJ Li - Bioinformatics, 2021 - academic.oup.com
Motivation Single-cell RNA sequencing (scRNA-seq) captures whole transcriptome
information of individual cells. While scRNA-seq measures thousands of genes, researchers …

Multiparametric assays for accelerating early drug discovery

A Herholt, S Galinski, PE Geyer, MJ Rossner… - Trends in …, 2020 - cell.com
Drug discovery campaigns are hampered by substantial attrition rates largely due to a lack
of efficacy and safety reasons associated with candidate drugs. This is true in particular for …

Potential of genomic selection and integrating “omics” data for disease evaluation in wheat

JK Haile, A N'Diaye, E Sari, S Walkowiak… - Crop Breeding …, 2020 - cbgg.hapres.com
Diseases are among the most important limiting factors for wheat production. Breeding for
fungal diseases of wheat, primarily for rusts and Fusarium head blight (FHB), are major …