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Status |
Public on Jun 24, 2023 |
Title |
Sterlet sturgeon scute 26mm, replicate two |
Sample type |
SRA |
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Source name |
cells of scute
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Organism |
Acipenser ruthenus |
Characteristics |
tissue: cells of scute genotype: WT measure: 26 mm
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Extracted molecule |
total RNA |
Extraction protocol |
RNAqueous kit (Ambion), prepared according to the manufacturer's instructions. The libraries were built according to Illumina Standard Protocols.
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 2500 |
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Description |
AR_scute_26mm_2 Sturgeon_scute_processed.txt
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Data processing |
In brief, every sterlet/bichir protein sequence was queried locally against the zebrafish proteome, following which regions with the longest alignment were matched to the respective zebrafish proteins. Using this alignment-based approach, proteins with highest alignment percentage score were identified as orthologues. Sterlet/bichir scute/scale RNA sequencing libraries were aligned to the sterlet/bichir sequences, while the zebrafish scale RNA sequencing libraries were aligned to the zebrafish sequences using Bowtie23. Transcript counts were calculated using featureCounts and differential gene expression analysis was performed using DESeq2. Using zebrafish gene annotations as a reference, we added the transcript counts for duplicated orthologues found in the sterlet/bichir genome to calculate an ‘aggregated’ transcript count for each gene as described by Martik et al., 2019. These aggregated transcript counts were then normalized using the formula: Zi=Ti−min(T)/max(T)−min(T) whereZiis the normalized transcript count andTiis the absolute transcript count. A subset of genes previously identified as being part of the neural crest gene regulatory network was then isolated from the count matrix and plotted as a heatmap using ComplexHeatmap package in Rstudio. Assembly: Sterlet sturgeon (Genome assembly ASM1064508v1)/ Senegal bichir (Genome assembly ASM1683550v1)/ zebrafish (Genome assembly GRCz11) Supplementary files format and content: tab-delimited text files that includes featurecounts values for each sample
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Submission date |
Jun 20, 2023 |
Last update date |
Jun 24, 2023 |
Contact name |
Jan Stundl |
E-mail(s) |
jstundl@caltech.edu
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Organization name |
California Institute of Technology
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Lab |
Bronner
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Street address |
1200 E. California Blvd
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City |
Pasadena |
State/province |
California |
ZIP/Postal code |
91125 |
Country |
USA |
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Platform ID |
GPL33508 |
Series (1) |
GSE235280 |
Ancient vertebrate dermal armor evolved from trunk neural crest |
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Relations |
BioSample |
SAMN35816074 |
SRA |
SRX20733644 |
Supplementary data files not provided |
SRA Run Selector |
Raw data are available in SRA |
Processed data are available on Series record |
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