2018
DOI: 10.1186/s12864-018-4840-5
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Correction to: De novo transcriptome assembly, annotation and comparison of four ecological and evolutionary model salmonid fish species

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Cited by 4 publications
(3 citation statements)
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“…Many of these have already been identified owing to transcriptome assembly in the brown trout (Carruthers et al, 2018) and consolidate resources to address this challenging key task. While the number of markers cannot be considered sufficient to accurate phylogeny estimation (Pyron, 2015) and their nature may lead to conflicting results (e.g., Reddy et al, 2017), results by Collins and Hrbek (2018) suggest good performance of SNP data coming from restriction-site-associated DNA (RAD) analysis to address relatively recent and shallow phylogenies.…”
Section: The Futurementioning
confidence: 99%
“…Many of these have already been identified owing to transcriptome assembly in the brown trout (Carruthers et al, 2018) and consolidate resources to address this challenging key task. While the number of markers cannot be considered sufficient to accurate phylogeny estimation (Pyron, 2015) and their nature may lead to conflicting results (e.g., Reddy et al, 2017), results by Collins and Hrbek (2018) suggest good performance of SNP data coming from restriction-site-associated DNA (RAD) analysis to address relatively recent and shallow phylogenies.…”
Section: The Futurementioning
confidence: 99%
“…(2019) Transcriptomics (RNA-seq, cDNA arrays, microarrays) Assembly of transcriptomic profiles Oncorhynchus mykiss; Salmo salar; Salmo trutta, Salvelinus alpinus, Coregonus lavaretus; Oncorhynchus tshawytscha Yes Salem et al. (2015) ; Carruthers et al. (2018) ; Christensen et al.…”
Section: Introductionmentioning
confidence: 99%
“…Next-generation sequencing (NGS; i.e., Illumina RNA sequencing) can generate digital data on gene expression without the limits of predesigned probes [6], and has been conducted not only to create the reference genomes such as in Arabidopsis [7], rice [8], maize [9], but also provides the de-novo assembly for many organisms in the past including animals and plants [10, 11]. The results of incomplete (ranging between 1 and 2 kb, including a methylated cap at the 5′ end and poly-A tails at the 3′ end) and low-quality transcripts obtained through Illumina RNA sequencing limit the scope of analysis of alternative splicing variants and corrected annotation [12].…”
Section: Introductionmentioning
confidence: 99%