2017
DOI: 10.1186/s12864-016-3448-x
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An improved genome assembly uncovers prolific tandem repeats in Atlantic cod

Abstract: BackgroundThe first Atlantic cod (Gadus morhua) genome assembly published in 2011 was one of the early genome assemblies exclusively based on high-throughput 454 pyrosequencing. Since then, rapid advances in sequencing technologies have led to a multitude of assemblies generated for complex genomes, although many of these are of a fragmented nature with a significant fraction of bases in gaps. The development of long-read sequencing and improved software now enable the generation of more contiguous genome asse… Show more

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Cited by 140 publications
(188 citation statements)
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“…0.20.4) (Schmieder and Edwards, 2011) (Supporting Information Table S15). PhiX, host and human sequences were removed by mapping reads to the phiX reference genome [GenBank: J02482.1], the Atlantic cod genome assembly (gadMor 2), (Tørresen et al, 2017) and a masked version of the human genome (HG19) (Genome Reference Consortium, 2009) using BWA (ver. 0.7.13) (Li and Durbin, 2009) or BBMap (ver.…”
Section: Sequence Data Generation and Filteringmentioning
confidence: 99%
“…0.20.4) (Schmieder and Edwards, 2011) (Supporting Information Table S15). PhiX, host and human sequences were removed by mapping reads to the phiX reference genome [GenBank: J02482.1], the Atlantic cod genome assembly (gadMor 2), (Tørresen et al, 2017) and a masked version of the human genome (HG19) (Genome Reference Consortium, 2009) using BWA (ver. 0.7.13) (Li and Durbin, 2009) or BBMap (ver.…”
Section: Sequence Data Generation and Filteringmentioning
confidence: 99%
“…Following this, sequence flanking each marker was 171 used to precisely position all genetic markers to contigs in the gadMor_Celtic 172 assembly using megablast (Altschul et al 1990), and thereby associate sequence 173 with linkage groups. This analysis revealed 2 chimeric contigs containing at 174 markers from each of different linkage groups that were selectively 'broken' 175 using alignments with the gadMor2 assembly (Torresen et al 2017 have directly compared reference genomes from different cod ecotypes to define 304 and confirm the underlying mechanism, or to locate the genomic regions 305 containing the inversion breakpoints or to define the exact complement of genes 306 they contain. We aligned the recently released gadMor3 assembly (NCBI 307 accession ID: GCF_902167405.1) constructed from a NEAC individual to our 308 gadMor_Celtic assembly using LASTZ (Harris 2007).…”
mentioning
confidence: 99%
“…We used the Drop-seq Core Computational Protocol (Namesh 2015) using STAR alignment to map the raw sequencing data to the most recent version of the Atlantic cod genome, gadMor3 (RefSeq accession GCF_902167405.1). A gene of interest, GATA-3, was present in gadMor2 (Torresen, Star et al 2017) but missing in gadMor3, so the GATA-3 gene sequence was manually added to the gadMor3 assembly fasta file. Reads were then grouped by cell barcode and the unique molecular identifiers (UMIs) for each gene counted, resulting in a digital expression matrix showing the number of transcripts per gene per cell.…”
Section: Quantification Of Genesmentioning
confidence: 99%