Searching journal content for articles similar to Sogayar and Camargo 14 (7): 1413.

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  1. ...and coverage across the full body of transcripts as important for future improvement, much work has been dedicated to reducing the error rate in long reads. However, the effect of sequencing errors on transcriptome analysis can be complex and context dependent. Correction algorithms like IsoQuant do not alter...
  2. ...Technologies to study the transcriptome complexity in Caenorhabditis elegans. We generated approximately six million reads using native poly(A)-tailed mRNAs from three developmental stages, with average read lengths ranging from 900 to 1100 nt. Around half of the reads represent full-length transcripts...
  3. ...and strongly suggest that even though theXenopus tropicalis is close to being finished, it is still missing hundreds of transcribed sequences. To determine if the Trinity contigs that could not be aligned to the are true transcripts or are simply spurious assemblies, we sought to validate some of them...
  4. ...for large-scale functional surveys. Two key methods have greatly enhanced our ability to assign functions to genes in systematic analyses: microarray transcript profiling ( Holloway et al. 2002 ) and silencing via RNA interference or RNAi ( Hannon 2002 ; Waterhouse and Helliwell 2003 ). Full transcriptome...
  5. ...alone may be not enough, especially if the organism shows a high degree of complexity. Analysis of the must be supported by efforts on understanding its transcription—the transcriptome—occurring in cells. Citing Camargo et al. ( 2001 ), the “most definitive approach to the elucidation of transcripts...
  6. ...tissues from both X. laevis and X. tropicalis ( Klein et al. 2002 ; Blackshear et al. 2001 ; Gilchrist et al. 2004 ). However, for analysis of transcripts and gene structures, the quality of data and coverage provided by EST reads can be limiting. Sequence-verified full-length cDNA clones are more...
  7. ...here) as well as protein similarity to build gene models. From this, 24,207 (85%) of the 28,416 Ensembl transcripts were matched, corresponding to 14,685 (83%) of the 17,709 Ensembl genes. The degree of transcriptome/ coverage based on these figures is comparable to that seen for the RIKEN...
  8. ...Research Center for Environment and Health, D-85764 Neuherberg, Germany; 2The Plant Genome Initiative at Rutgers (PGIR), Waksman Institute, Rutgers, The State University of New Jersey, Piscataway, New Jersey 08854, USA; 3Broad Institute of MIT and Harvard, Cambridge, Massachusetts...
  9. ...-seq) on peripheral blood mononuclear cells (PBMCs) from the donor (Ford et al. 2023). Notably, we identified productive transcripts from both copies of IGHA1 and IGHG2 within the duplicated haplotype 1 (Fig. 5C). Because the centromeric copy of IGHG4 on haplotype 1 is identical to that on haplotype 2, calling...
  10. ..., even though the RNA-seq data were collected in two independent studies, supporting the presence of transcription.DiscussionUsing high-accuracy PacBio HiFi and ultralong Oxford Nanopore long-read sequencing, as well as augmenting our initial HiCanu assembly with manual assembly of 54 tandemly repeated...
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