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Status |
Public on Sep 13, 2020 |
Title |
B724-1 |
Sample type |
SRA |
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Source name |
Candida auris
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Organism |
Candidozyma auris |
Characteristics |
genotype: Diploid
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Growth protocol |
YPD medium and cultured at 30 oC for 12h.
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Extracted molecule |
total RNA |
Extraction protocol |
Cells were lysed by Mini-beadbeater and total RNA was harvested using GeneJET RNA Purification Kit (Thermo Scientific #K0731, #K0732) RNA libraries were prepared for sequencing using standard Illumina protocols
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NovaSeq 6000 |
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Data processing |
Illumina OLB_1.9.4 were used for basecalling Filter dirty raw reads by removing reads with adaptors and low quality, the obtained clean reads were mapped to reference sequences using SOAPaligner/soap2 according to Li et al., Bioinformatics, 2009. Mismatches no more than 2 bases were allowed in the alignment. The gene expression level is calculated by using FPKM method (Reads Per kb per Million reads) according to Mortazavi, et a., Nature Methods, 2008, and the formula is shown as follows: FPKM=106C/(NL/103). C is the number of reads that uniquely aligned to a gene, N is total number of reads that uniquely aligned to all genes, and L is the number of bases on a gene . Genome_build: Candida auris genome Supplementary_files_format_and_content: text files containing FPKM values for each Sample
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Submission date |
Apr 24, 2020 |
Last update date |
Sep 13, 2020 |
Contact name |
Jian Bing |
E-mail(s) |
bingj@fudan.edu.cn
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Organization name |
Fudan University
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Department |
School of Life Sciences
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Street address |
Songhu Road, Yangpu District
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City |
Shanghai |
ZIP/Postal code |
200438 |
Country |
China |
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Platform ID |
GPL28368 |
Series (1) |
GSE149284 |
Haploid and Deploid for Candida auris |
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Relations |
BioSample |
SAMN14689137 |
SRA |
SRX8171345 |
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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