data net seq Search Results


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SourceForge net computational pipeline for ribofr-seq data analyses
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SourceForge net gene prediction (hmm-based) using both rna-seq data and genome sequence
Gene Prediction (Hmm Based) Using Both Rna Seq Data And Genome Sequence, supplied by SourceForge net, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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SourceForge net python-based suite to process raw rna-seq or exome-seq data for customized database construction
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SourceForge net computational pipeline for processing o2n-seq data
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SourceForge net pipeline for rna-seq data analysis (prada)
Pipeline For Rna Seq Data Analysis (Prada), supplied by SourceForge net, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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SourceForge net rna-seq raw data fastq files
<t>RNA-seq</t> analysis and validation of DE genes specific to StMSI1-OE or StBMI1-1-AS line. A, Venn diagram shows the summary of DE genes in StMSI1-OE and StBMI1-AS lines compared to VC line. B and C, Validation of selective StMSI1-specific (B) and StBMI1-1-specific genes (C) compared to VC. The relative fold-change of respective gene expression in StMSI1-OE or StBMI1-1-AS lines was calculated with respect to its transcript level in VC plant. Student’s t test was performed to check significance with *P < 0.05, **P < 0.01, ***P < 0.001, and ****P < 0.0001. ns, not significant. Error bars represent ± sd from three biological and three technical replicates. EIF3e was used as a reference gene.
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SourceForge net simulated and pre-processed chip-seq data
<t>RNA-seq</t> analysis and validation of DE genes specific to StMSI1-OE or StBMI1-1-AS line. A, Venn diagram shows the summary of DE genes in StMSI1-OE and StBMI1-AS lines compared to VC line. B and C, Validation of selective StMSI1-specific (B) and StBMI1-1-specific genes (C) compared to VC. The relative fold-change of respective gene expression in StMSI1-OE or StBMI1-1-AS lines was calculated with respect to its transcript level in VC plant. Student’s t test was performed to check significance with *P < 0.05, **P < 0.01, ***P < 0.001, and ****P < 0.0001. ns, not significant. Error bars represent ± sd from three biological and three technical replicates. EIF3e was used as a reference gene.
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RNA-seq analysis and validation of DE genes specific to StMSI1-OE or StBMI1-1-AS line. A, Venn diagram shows the summary of DE genes in StMSI1-OE and StBMI1-AS lines compared to VC line. B and C, Validation of selective StMSI1-specific (B) and StBMI1-1-specific genes (C) compared to VC. The relative fold-change of respective gene expression in StMSI1-OE or StBMI1-1-AS lines was calculated with respect to its transcript level in VC plant. Student’s t test was performed to check significance with *P < 0.05, **P < 0.01, ***P < 0.001, and ****P < 0.0001. ns, not significant. Error bars represent ± sd from three biological and three technical replicates. EIF3e was used as a reference gene.

Journal: Plant Physiology

Article Title: PcG Proteins MSI1 and BMI1 Function Upstream of miR156 to Regulate Aerial Tuber Formation in Potato 1 [OPEN]

doi: 10.1104/pp.19.00416

Figure Lengend Snippet: RNA-seq analysis and validation of DE genes specific to StMSI1-OE or StBMI1-1-AS line. A, Venn diagram shows the summary of DE genes in StMSI1-OE and StBMI1-AS lines compared to VC line. B and C, Validation of selective StMSI1-specific (B) and StBMI1-1-specific genes (C) compared to VC. The relative fold-change of respective gene expression in StMSI1-OE or StBMI1-1-AS lines was calculated with respect to its transcript level in VC plant. Student’s t test was performed to check significance with *P < 0.05, **P < 0.01, ***P < 0.001, and ****P < 0.0001. ns, not significant. Error bars represent ± sd from three biological and three technical replicates. EIF3e was used as a reference gene.

Article Snippet: RNA-seq raw data FASTQ files ( http://maq.sourceforge.net/fastq.shtml ) generated from this study were deposited and available at the National Centre for Biotechnology Information Sequence Read Archive ( https://www.ncbi.nlm.nih.gov/sra ) under accession number PRJNA546591.

Techniques: RNA Sequencing Assay, Expressing