the transcripts and utilized for functional annotation. We mapped the predicted proteins to 304 known

the transcripts and utilized for functional annotation. We mapped the predicted proteins to 304 known KEGG pathways with signal transduction cluster having the highest representation followed by immune technique and endocrine method. In addition, transcripts exhibiting considerable similarity to previously VEGFR3/Flt-4 drug AChE Activator Molecular Weight Published growth-and immune-related genes were identified that will facilitate future molecular breeding of Tor tambra.Report history: Received three June 2021 Revised 17 September 2021 Accepted 7 October 2021 Readily available on line 14 October 2021 Keywords: Transcriptome Unigenes Gene annotation Tor tambraCorresponding Author. E-mail address: [email protected] (H.H. Chung).doi.org/10.1016/j.dib.2021.107481 2352-3409/2021 The Author(s). Published by Elsevier Inc. This can be an open access write-up beneath the CC BY license (http://creativecommons.org/licenses/by/4.0/)M.M.L. Lau, L.W.K. Lim and H.H. Chung et al. / Information in Short 39 (2021)2021 The Author(s). Published by Elsevier Inc. This really is an open access report under the CC BY license (http://creativecommons.org/licenses/by/4.0/)Specifications TableSubject Certain topic location Sort of data How data were acquired Data format Parameters for data collection Description of data collection Biological Sciences Omics: Transcriptomics Sequencing raw reads, assembly, Table, Figure, Graph Sequencing Raw Reads (fastq), Assembly (fasta) Total RNA extracted from a complete specimen of fish fry was used for library preparation and sequencing. Total RNA extraction was performed working with Wizol TriZol-like reagent (WizBio). The purified total RNA was subjected to mRNA enrichment applying poly-T magnetic bead (NEB). The enriched mRNA was subsequently processed applying NEB Ultra II RNA library preparation kit and sequenced on an Illumina NovaSeq60 0 0 (2 150 bp) The sample fish fry in this study was supplied by a fish breeder who claimed that it originated from the Pahang, Malaysia. We subsequently extracted the mitochondrial genes in the transcriptome and showed that this specimen certainly formed a monophyletic cluster with Tor spp described from Pahang, Malaysia (Fig. 1) [1]. Raw information and final assembled contigs had been deposited in the NCBI database under the Bioproject PRJNA727425 (ncbi.nlm.nih.gov/bioproject/PRJNA727425). Added files such as BUSCO analysis output, GO annotation, KEGG annotation and COG annotation are offered inside the Zenodo database doi.org/10.5281/zenodo.4766490.Data source locationData accessibilityValue of the Information Transcriptome dataset from the Javan mahseer is valuable to achieve insight into transcription regulation and biomarker discovery for the subsequent improvement of this species for aquaculture purposes. High completeness of transcriptome dataset will help in future phylotranscriptomic studies especially for fish taxonomist. The dataset is useful in facilitating genetic management for the conservation of remaining populations of mahseer in Malaysian rivers.1. Information Description Standard RNA sequencing was performed to produce the transcriptome assembly from Javan mahseer (Tor tambra). Sequencing and assembly results are summarized in Table 1. Coding area was extracted employing TransDecoder creating 77,503 predicted non-redundant proteins [2]. The proteins had been annotated applying eggNOG mapper [3] that could carry out mapping for the KEGG, GO and COG databases. The sequence length of each unigene ranged from 300 bp to 50 0 0 bp (Fig. 2). The amount of unigenes had shown a decreasing trend when the length incr