Publications by authors named "P A Doris"

Article Synopsis
  • A new reference genome assembly for the laboratory rat, named GRCr8, has been developed and is recognized by the Genome Reference Consortium.
  • The assembly utilized advanced sequencing techniques (40× PacBio HiFi sequencing) and includes chromosome-level data, with 98.7% of sequences assigned to chromosomes, showing overall increases in chromosome sizes and notable expansions on Chromosomes 3, 11, 12, and Chr Y.
  • The new assembly enhances genome quality by incorporating over 1100 new protein-coding genes and includes previously unannotated genes and centromeric sequences, supported by concurrent PacBio Iso-Seq data from multiple rat tissues.
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Article Synopsis
  • * New genetic studies have created a better version of the rat's DNA map, called GRCr8, which is more accurate and includes new information.
  • * As technology improves, researchers are now able to make more detailed DNA maps of different rat breeds, helping to unlock even more secrets about their genetics.
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The seventh iteration of the reference genome assembly for Rattus norvegicus-mRatBN7.2-corrects numerous misplaced segments and reduces base-level errors by approximately 9-fold and increases contiguity by 290-fold compared with its predecessor. Gene annotations are now more complete, improving the mapping precision of genomic, transcriptomic, and proteomics datasets.

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During development of the spontaneously hypertensive rat (SHR), several distinct but closely related lines were generated. Most lines are resistant to hypertensive renal disease. However, the SHR-A3 line (stroke-prone SHR) experiences end-organ injury (EOI) and provides a model of injury susceptibility that can be used to uncover genetic causation.

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The seventh iteration of the reference genome assembly for -mRatBN7.2-corrects numerous misplaced segments and reduces base-level errors by approximately 9-fold and increases contiguity by 290-fold compared to its predecessor. Gene annotations are now more complete, significantly improving the mapping precision of genomic, transcriptomic, and proteomics data sets.

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