Searching journal content for articles similar to Prasad et al. 27 (1): 133.

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  1. ...-performing one (Supplemental Fig. S5B). When reference data are limited, CAMUS can incorporate reference-integrated approaches, namely, the multi-ref and ensemble, to achieve better annotations.CAMUS enables highly accurate method selection for scST and scATAC-seq dataWe further applied CAMUS to 80 scST and five...
  2. ...310022, China; 9State Key Laboratory for Macromolecule Drugs and Large-scale Manufacturing, School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou 325030, China ↵10 These authors contributed equally to this work. Corresponding authors: wuyf@immunol.org, reny@genomics.cn, jingang...
  3. ..., Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA Corresponding author: borodovsky@gatech.eduAbstractLarge-scale genomic initiatives, such as the Earth BioGenome Project, require efficient methods for eukaryotic annotation. Here we present an automatic gene finder, GeneMark-ETP, integrating...
  4. ...category, and the user has the option to explore the full set of G4s for each with additional annotations.Quadrupia offers experimental validation for the G4 sequences of selected s in three forms: (1) genomic coordinate matches to experimentally validated G4 sequences, as described in the study by Marsico...
  5. ...properties and functions, and are promising biomarkers. Existing methods for assembling circRNAs heavily rely on the annotated transcriptomes, hence exhibiting unsatisfactory accuracy without a high-quality transcriptome. We present TERRACE, a new algorithm for full-length assembly of circRNAs from paired...
  6. ...have the potential of discarding real biological TD from less abundant transcripts or those present in sample-specific conditions. Therefore, developing accurate algorithms to identify TD represents a new and important challenge for the computational biology and RNA communities.Genome annotation...
  7. ...Evaluation of strategies for evidence-driven annotation using long-read RNA-seq Alejandro Paniagua1,2,6, Cristina Agustín-García1,6, Francisco J. Pardo-Palacios1, Thomas Brown3,4, Maite De Maria5, Nancy D. Denslow5, Camila J. Mazzoni3,4 and Ana Conesa1 1Institute for Integrative Systems Biology...
  8. ...@bcm.eduAbstractThe vast majority of protein-coding genes in the human produce multiple mRNA isoforms through alternative splicing, significantly enhancing the complexity of the transcriptome and proteome. To establish an efficient method for characterizing transcript isoforms within tissue samples, we conducted...
  9. ..., posing challenges for accurate pathway analysis. To address this issue, we introduce SiPSiC, a new tool designed to calculate pathway scores for each individual cell and each gene set by using gene expression values normalized by the expression levels in other cells and weighted by the rank...
  10. ...transcriptomes and proteomes vary across s, between genes, and even along a single gene. User-friendly and accurate annotation pipelines that can cope with such data heterogeneity are needed. The previously developed annotation pipelines BRAKER1 and BRAKER2 use RNA-seq or protein data, respectively, but not both...
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