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Status |
Public on Jun 04, 2018 |
Title |
Gibbon_DAICHI_DPFC |
Sample type |
SRA |
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Source name |
dorsolateral prefrontal cortex
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Organism |
Hylobates lar |
Characteristics |
individual id: DAICHI age (year): 9 Sex: male rin: 6.3 processing date: 20130408
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Extracted molecule |
polyA RNA |
Extraction protocol |
Brain dissection was performed from either fresh specimens or frozen tissue slabs by the same person to ensure sampling consistency between specimens. About 100 mg of dissected tissues were used and total RNA were extracted using RNeasy Plus Universal Kit (Qiagen). Quality and quantity measurements of extracted RNA were performed using NanoDrop (Thermo Fisher Scientific) and Qubit Fluorometer (Thermo Fisher Scientific), respectively, and the RNA Integrity Number (RIN) were determined using Bioanalyzer RNA 6000 Nano Kit (Agilent). Sequencing libraries were prepared using the NEBNext mRNA Library Prep Kit for non-directional libraries and the NEBNext Ultra Directional RNA Library Prep Kit for directional libraries (New England BioLabs) according to the manufacturer’s instructions.
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 2000 |
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Data processing |
Raw reads of four species were aligned to the reference genomes (human, hg19; chimpanzee, panTro4; gorilla, gorGor3; gibbon, nomLeu1) by “STAR” (parameters: outFilterMultimapNmax = 1, outFilterMatchNminOverLread = 0.95, outFilterMismatchNoverLmax = 0.05, outFilterIntronMotifs = RemoveNoncanonical). PCR duplicates removal was then conducted using SAMtools and only uniquely mapped reads were considered as validity to avoid the estimation ambiguity. We obtained chimpanzee, gorilla and gibbon orthologs of human genes (GENCODE v19) by reciprocal liftOver requiring the same exon orders and no less than 50% exons preserved. Based on the annotations, numbers of reads were counted per gene per sample using htseq-count within HTSeq. Only genes with counts greater than 0 in all four species in at least one brain region were used in the following analysis We took advantage of the median ratio method implemented in DESeq2 to normalize the gene abundance data for further comparisons across species and brain regions. Genome_build: human, hg19; chimpanzee, panTro4; gorilla, gorGor3; gibbon, nomLeu1 Supplementary_files_format_and_content: tab-delimited text files include raw count, normalized count, and RPKM for each sample
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Submission date |
Jul 05, 2017 |
Last update date |
May 15, 2019 |
Contact name |
Yasuhiro Go |
E-mail(s) |
yasuhirogo@gmail.com
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Organization name |
National Institutes of Natural Sciences
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Department |
Department of Brain Sciences, Center for Novel Science Initiatives
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Street address |
38 Nishigonaka Myodaiji
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City |
Okazaki |
ZIP/Postal code |
4448585 |
Country |
Japan |
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Platform ID |
GPL23664 |
Series (1) |
GSE100796 |
Human-specific features of special gene expression and regulation in eight brain regions |
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Relations |
BioSample |
SAMN07315626 |
SRA |
SRX2983722 |
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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