Search Results - "Jabbari, Jafar S"
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Benchmarking UMI-based single-cell RNA-seq preprocessing workflows
Published in Genome Biology (14-12-2021)“…Single-cell RNA-sequencing (scRNA-seq) technologies and associated analysis methods have rapidly developed in recent years. This includes preprocessing…”
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Actinobacillus pleuropneumoniae encodes multiple phase-variable DNA methyltransferases that control distinct phasevarions
Published in Nucleic acids research (24-04-2023)“…Abstract Actinobacillus pleuropneumoniae is the cause of porcine pleuropneumonia, a severe respiratory tract infection that is responsible for major economic…”
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Genome assembly of the Australian black tiger shrimp (Penaeus monodon) reveals a novel fragmented IHHNV EVE sequence
Published in G3 : genes - genomes - genetics (04-04-2022)“…Shrimp are a valuable aquaculture species globally; however, disease remains a major hindrance to shrimp aquaculture sustainability and growth. Mechanisms…”
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scPipe: an extended preprocessing pipeline for comprehensive single-cell ATAC-Seq data integration in R/Bioconductor
Published in NAR genomics and bioinformatics (01-12-2023)“…Abstract scPipe is a flexible R/Bioconductor package originally developed to analyse platform-independent single-cell RNA-Seq data. To expand its preprocessing…”
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The First Genetic Map for a Psoraleoid Legume (Bituminaria bituminosa) Reveals Highly Conserved Synteny with Phaseoloid Legumes
Published in Plants (Basel) (31-07-2020)“…We present the first genetic map of tedera (Bituminaria bituminosa (L.) C.H. Stirton), a drought-tolerant forage legume from the Canary Islands with useful…”
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Benchmarking single cell RNA-sequencing analysis pipelines using mixture control experiments
Published in Nature methods (01-06-2019)“…Single cell RNA-sequencing (scRNA-seq) technology has undergone rapid development in recent years, leading to an explosion in the number of tailored data…”
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High concordance between Illumina HiSeq2500 and NextSeq500 for reduced representation bisulfite sequencing (RRBS)
Published in Genomics data (01-12-2016)“…Reduced representation bisulfite sequencing (RRBS) provides an efficient method for measuring DNA methylation at single base resolution in regions of high CpG…”
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A single‐cell transcriptome atlas of the adult human retina
Published in The EMBO journal (16-09-2019)“…The retina is a specialized neural tissue that senses light and initiates image processing. Although the functional organization of specific retina cells has…”
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Single-cell multiomics reveal the scale of multilayered adaptations enabling CLL relapse during venetoclax therapy
Published in Blood (17-11-2022)“…•Multiple independent but recurring genetic and epigenetic changes drive venetoclax resistance, with marked NF-κB activation ubiquitous.•NF-κB activation is…”
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Benchmarking long-read RNA-sequencing analysis tools using in silico mixtures
Published in Nature methods (01-11-2023)“…The lack of benchmark data sets with inbuilt ground-truth makes it challenging to compare the performance of existing long-read isoform detection and…”
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Comprehensive characterization of single-cell full-length isoforms in human and mouse with long-read sequencing
Published in Genome Biology (11-11-2021)“…A modified Chromium 10x droplet-based protocol that subsamples cells for both short-read and long-read (nanopore) sequencing together with a new computational…”
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Single cell RNA sequencing of stem cell-derived retinal ganglion cells
Published in Scientific data (13-02-2018)“…We used single cell sequencing technology to characterize the transcriptomes of 1,174 human embryonic stem cell-derived retinal ganglion cells (RGCs) at the…”
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Targeting histone acetylation dynamics and oncogenic transcription by catalytic P300/CBP inhibition
Published in Molecular cell (20-05-2021)“…To separate causal effects of histone acetylation on chromatin accessibility and transcriptional output, we used integrated epigenomic and transcriptomic…”
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Fatal perinatal mitochondrial cardiac failure caused by recurrent de novo duplications in the ATAD3 locus
Published in Med (New York, N.Y. : Online) (15-01-2021)“…In about half of all patients with a suspected monogenic disease, genomic investigations fail to identify the diagnosis. A contributing factor is the…”
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