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The genome refers to all of the genetic material in an organism. It can range from a few million base pairs in microbial cells to several billion base pairs in many eukaryotic organisms. Genome assembly refers to the process of taking the DNA sequencing data and putting it all back together in a correct order to create a close representation of the original genome. This is followed by the identification of functional elements on the newly assembled genome, a process called genome annotation.
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Genomics is the science of genomes: it is the study of all the genetic material of an organism. In humans, the genome consists of information carried in 23 pairs of chromosomes in the nucleus, as well as mitochondrial DNA. In genomics, both coding and non-coding DNA is sequenced and analyzed. Genomics allows a better understanding of all living things, their evolution, and their diversity. It has a myriad of uses: for example, to build phylogenetic trees, to improve productivity and...
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Diploid organisms inherit genetic material through chromosomes from both parents. Copies of the same gene are known as alleles. In most cases, both alleles are simultaneously expressed and allow various cellular processes to function optimally. If one of the alleles is missing or mutated, the expression of the other allele can compensate; however, this is not true for all genes.
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While every living organism has a genome of some kind (be it RNA, or DNA), there is considerable variation in the sizes of these blueprints. One major factor that impacts genome size is whether the organism is prokaryotic or eukaryotic. In prokaryotes, the genome contains little to no non-coding sequence, such that genes are tightly clustered in groups or operons sequentially along the chromosome. Conversely, the genes in eukaryotes are punctuated by long stretches of non-coding sequence.
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The present-day mitochondrial and chloroplast genomes have retained some of the characteristics of their ancestral prokaryotes and also have acquired new attributes during their evolution within eukaryotic cells. Like prokaryotic genomes, mitochondrial and chloroplast genomes neither bind with histone-like proteins nor show complex packaging into chromosome-like structures, as observed in eukaryotes. Unlike mitotic cell divisions observed in eukaryotic cells, mitochondria and chloroplasts...
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BarkBase: Epigenomic Annotation of Canine Genomes.

Kate Megquier1, Diane P Genereux2, Jessica Hekman3

  • 1Vertebrate Genomics, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA. kmegq@broadinstitute.org.

Genes
|June 12, 2019
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Summary

Researchers created BarkBase, a canine epigenomic resource, to better understand dog genetics and complex diseases like cancer. This new database provides crucial canine-specific genomic data for improved disease research and comparative studies.

Keywords:
ATAC-seqRNA-seqannotationcaninecomparativedogepigenomicexpressiongenome

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Area of Science:

  • Genomics
  • Comparative Biology
  • Canine Genetics

Background:

  • Dogs serve as valuable natural models for studying complex diseases, including cancer.
  • Accurate genomic annotation of regulatory elements in healthy canine tissues is essential for identifying disease-causing genetic variants.
  • Current canine genetic research often relies on remapped human or mouse genome annotations, which may miss dog-specific genomic features.

Purpose of the Study:

  • To introduce BarkBase, a comprehensive canine epigenomic resource.
  • To provide dog-specific genomic data for regulatory elements across various tissues and developmental stages.
  • To facilitate comparative genomic studies between dogs and humans.

Main Methods:

  • Collected RNA sequencing and whole genome sequencing data from 27 adult canine tissues and four embryonic time points.
  • Utilized Assay for Transposase-Accessible Chromatin using sequencing (ATAC-seq) to identify open chromatin regions.
  • Incorporated biological replicates to enhance the accuracy of transcript and gene expression analysis.

Main Results:

  • BarkBase offers extensive epigenomic data for 27 adult tissues and embryonic samples.
  • The resource includes RNA sequencing, whole genome sequencing, and ATAC-seq data.
  • Data is available in user-friendly formats with a visual browser for easy access and analysis.

Conclusions:

  • BarkBase is a powerful new resource for canine genetic research, offering dog-specific epigenomic information.
  • The resource supports the identification of candidate causal variants and the design of functional studies for canine diseases.
  • BarkBase enables robust comparative studies, advancing our understanding of both canine and human health and disease genetics.