Comprehensive de novo mutation discovery with HiFi long-read sequencing.
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Genetic Techniques
701 articles with social media discussions tracked by PubHawk in this topic.
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Predictive and robust gene selection for spatial transcriptomics.
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Consequences and opportunities arising due to sparser single-cell RNA-seq datasets.
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Immune cell dynamics deconvoluted by single-cell RNA sequencing in normothermic machine perfusion of the liver.
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Whole exome sequencing analysis of canine urothelial carcinomas without BRAF V595E mutation: Short in-frame deletions in BRAF and MAP2K1 suggest alternative mechanisms for MAPK pathway disruption.
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Improved analysis of (e)CLIP data with RCRUNCH yields a compendium of RNA-binding protein binding sites and motifs.
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Spatially informed clustering, integration, and deconvolution of spatial transcriptomics with GraphST.
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An integrated single cell and spatial transcriptomic map of human white adipose tissue.
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A comprehensive benchmarking with practical guidelines for cellular deconvolution of spatial transcriptomics.
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The shaky foundations of simulating single-cell RNA sequencing data.
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RNA splicing analysis using heterogeneous and large RNA-seq datasets.
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Is there a placental microbiota? A critical review and re-analysis of published placental microbiota datasets.
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An integrated single-cell transcriptomic dataset for non-small cell lung cancer.
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FLI1 and FRA1 transcription factors drive the transcriptional regulatory networks characterizing muscle invasive bladder cancer.
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Optogenetic rejuvenation of mitochondrial membrane potential extends lifespan.
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Single-cell RNA sequencing reveals homogeneous transcriptome patterns and low variance in a suspension CHO-K1 and an adherent HEK293FT cell line in culture conditions.
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Cross-platform normalization enables machine learning model training on microarray and RNA-seq data simultaneously.
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Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains.
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Psammomatoid Ossifying Fibroma Is Defined by SATB2 Rearrangement.
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Systematic optimization of Cas12a base editors in wheat and maize using the ITER platform.
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Genome-wide analysis of aberrant position and sequence of plasma DNA fragment ends in patients with cancer.
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On AIRR 8: Engineering B cells or Giving the immune System an Optimal Starting Point with Dr. Barzel
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Prediction of designer-recombinases for DNA editing with generative deep learning.
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SARS-CoV-2 Omicron variant shows less efficient replication and fusion activity when compared with Delta variant in TMPRSS2-expressed cells.
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