Conserved regulation of RNA processing in somatic cell reprogramming
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<strong>Data set 1. Transcript expression across human RNA-Seq samples: estimated read counts. </strong>The file contains estimated read counts, generated by kallisto (https://pachterlab.github.io/kallisto/), for human transcripts and RNA-Seq samples used in this study (see Additional file 2 of the accompanying publication). The format is a compressed (GZIP) tab-separated transcript-by-sample matrix. Ensembl transcript identifiers and a combined Sequence Read Archive study/sample name identifier serve as row and column names, respectively.
<strong>Data set 2. Transcript expression across murine RNA-Seq samples: estimated read counts. </strong>As in Data set 1, but for mouse transcripts.
<strong>Data set 3. Transcript expression across simian RNA-Seq samples: estimated read counts. </strong>As in Data set 1, but for chimpanzee transcripts.
<strong>Data set 4. Transcript expression across across human RNA-Seq samples: estimated transcript abundances. </strong>As in Data set 1, but instead of read counts, transcript abundances in transcripts per million (TPM), as estimated by kallisto (https://pachterlab.github.io/kallisto/), are listed. Format, column and row names as in Data set 1.
<strong>Data set 5. Transcript expression across murine RNA-Seq samples: estimated transcript abundances. </strong>As in Data set 4, but for mouse transcripts.
<strong>Data set 6. Transcript expression across simian RNA-Seq samples: estimated transcript abundances. </strong>As in Data set 4, but for chimpanzee transcripts.
<strong>Data set 7. Differential expression analyses across human RNA-Seq sample groups: log fold changes. </strong>The file contains log fold changes, inferred by edgeR (http://bioconductor.org/packages/release/bioc/html/edgeR.html), for human genes and the RNA-Seq sample group contrasts listed in Additional file 3 of the accompanying publication in a compressed (GZIP) TSV gene-by-comparison matrix. Ensembl gene identifiers and a descriptive contrast identifier serve as row and column names, respectively.
<strong>Data set 8. Differential expression analyses across murine RNA-Seq sample groups: log fold changes. </strong>As in Data set 7, but for mouse genes.
<strong>Data set 9. Differential expression analyses across simian RNA-Seq sample groups: log fold changes. </strong>As in Data set 7, but for chimpanzee genes.
<strong>Data set 10. Differential expression analyses across human RNA-Seq sample groups: false discovery rates. </strong>The file contains false discovery rates (FDR) for the differential expression analyses summarized in Data set 7. Format, column and row names as in Data set 7.
<strong>Data set 11. Differential expression analyses across murine RNA-Seq sample groups: false discovery rates. </strong>As in Data set 10, but for mouse genes.
<strong>Data set 12. Differential expression analyses across simian RNA-Seq sample groups: false discovery rates. </strong>As in Data set 10, but for chimpanzee genes.
<strong>Data set 13. Quantification of alternative splicing events across human RNA-Seq samples. </strong>The file contains ‘percent spliced in’ (PSI) values computed by SUPPA (https://github.com/comprna/SUPPA) for annotated alternative splicing events (inferred from the transcript annotation of the human genome, Ensembl release 84; http://www.ensembl.org/). The format is a compressed (GZIP) tab-separated transcript-by-sample matrix. SUPPA-provided event identifiers and a combined Sequence Read Archive study/sample name identifier serve as row and column names, respectively.
<strong>Data set 14. Quantification of alternative splicing events across murine RNA-Seq samples. </strong>As in Data set 13, but for mouse alternative splicing events.
<strong>Data set 15. Differential splicing analyses across human RNA-Seq sample groups: differences in ‘percent spliced in’ (ΔPSI). </strong>The file contains ΔPSI values for human alternative splicing events (as in Data set 13). The RNA-Seq sample group contrasts are listed in Additional file 3 of the accompanying publication. Values were inferred by SUPPA’s diffSplice functionality (https://github.com/comprna/SUPPA). The format is a compressed (GZIP) tab-separated gene-by-comparison matrix. SUPPA event identifiers and a descriptive contrast identifier serve as row and column names, respectively.
<strong>Data set 16. Differential splicing analyses across murine RNA-Seq sample groups: differences in ‘percent spliced in’ (ΔPSI). </strong>As in Data set 15, but for mouse alternative splicing events.
<strong>Data set 17. Differential splicing analyses across human RNA-Seq sample groups: P values. </strong>The file contains P values for the differential splicing analysis of human alternative splicing events summarized in Data set 15. Format, column and row names as in Data set 15.
<strong>Data set 18. Differential splicing analyses across murine RNA-Seq sample groups: P values. </strong>The file contains P values for the differential splicing analysis of mouse alternative splicing events summarized in Data set 16. Format, column and row names as in Data set 15.
<strong>Data set 19. Transcript expression across murine RNA-Seq time course data: estimated read counts. </strong>As in Data set 2, but for the time course data generated for the accompanying publication.
<strong>Data set 20. Transcript expression across murine RNA-Seq time course data: estimated transcript abundances. </strong>As in Data set 5, but for the time course data generated for the accompanying publication.
<strong>Data set 21. Quantification of alternative splicing events across murine RNA-Seq time course data. </strong>As in Data set 14, but for the time course data generated for the accompanying publication.
<strong>数据集1:人类RNA测序(RNA-Seq)样本转录本表达:估算读取计数</strong>
本文件包含本研究使用的人类转录本与RNA-Seq样本的估算读取计数,由kallisto(https://pachterlab.github.io/kallisto/)生成(详见配套发表论文的补充材料2)。文件格式为经GZIP压缩的制表符分隔转录本-样本矩阵。行名与列名分别为Ensembl转录本标识符,以及组合式序列读取存档(Sequence Read Archive, SRA)研究/样本名称标识符。
<strong>数据集2:小鼠RNA测序(RNA-Seq)样本转录本表达:估算读取计数</strong>
与数据集1一致,但针对小鼠转录本。
<strong>数据集3:灵长类RNA测序(RNA-Seq)样本转录本表达:估算读取计数</strong>
与数据集1一致,但针对黑猩猩转录本。
<strong>数据集4:人类RNA测序(RNA-Seq)样本转录本表达:估算转录本丰度</strong>
与数据集1一致,但此处列出的是由kallisto估算的、以每百万转录本(transcripts per million, TPM)为单位的转录本丰度,而非读取计数。文件格式、行名与列名均与数据集1相同。
<strong>数据集5:小鼠RNA测序(RNA-Seq)样本转录本表达:估算转录本丰度</strong>
与数据集4一致,但针对小鼠转录本。
<strong>数据集6:灵长类RNA测序(RNA-Seq)样本转录本表达:估算转录本丰度</strong>
与数据集4一致,但针对黑猩猩转录本。
<strong>数据集7:人类RNA测序样本组的差异表达分析:对数折叠变化</strong>
本文件包含由edgeR(http://bioconductor.org/packages/release/bioc/html/edgeR.html)推导得到的人类基因对数折叠变化,对应配套发表论文补充材料3中列出的RNA-Seq样本组对比,格式为经GZIP压缩的制表符分隔基因-对比矩阵。行名与列名分别为Ensembl基因标识符,以及描述性对比标识符。
<strong>数据集8:小鼠RNA测序样本组的差异表达分析:对数折叠变化</strong>
与数据集7一致,但针对小鼠基因。
<strong>数据集9:灵长类RNA测序样本组的差异表达分析:对数折叠变化</strong>
与数据集7一致,但针对黑猩猩基因。
<strong>数据集10:人类RNA测序样本组的差异表达分析:错误发现率(false discovery rate, FDR)</strong>
本文件包含数据集7中汇总的人类差异表达分析的错误发现率(FDR)。文件格式、行名与列名均与数据集7相同。
<strong>数据集11:小鼠RNA测序样本组的差异表达分析:错误发现率</strong>
与数据集10一致,但针对小鼠基因。
<strong>数据集12:灵长类RNA测序样本组的差异表达分析:错误发现率</strong>
与数据集10一致,但针对黑猩猩基因。
<strong>数据集13:人类RNA测序样本可变剪接事件定量</strong>
本文件包含由SUPPA(https://github.com/comprna/SUPPA)计算得到的、针对注释可变剪接事件的剪接百分比(percent spliced in, PSI)值(可变剪接事件由人类基因组转录本注释推导而来,对应Ensembl发布84版;http://www.ensembl.org/)。文件格式为经GZIP压缩的制表符分隔转录本-样本矩阵。行名与列名分别为SUPPA提供的事件标识符,以及组合式序列读取存档(SRA)研究/样本名称标识符。
<strong>数据集14:小鼠RNA测序样本可变剪接事件定量</strong>
与数据集13一致,但针对小鼠可变剪接事件。
<strong>数据集15:人类RNA测序样本组的差异剪接分析:剪接百分比差值(ΔPSI)</strong>
本文件包含人类可变剪接事件的ΔPSI值(同数据集13),对应RNA-Seq样本组对比详见配套发表论文补充材料3。该数值由SUPPA的diffSplice功能(https://github.com/comprna/SUPPA)推导得到。文件格式为经GZIP压缩的制表符分隔基因-对比矩阵。行名与列名分别为SUPPA事件标识符,以及描述性对比标识符。
<strong>数据集16:小鼠RNA测序样本组的差异剪接分析:剪接百分比差值(ΔPSI)</strong>
与数据集15一致,但针对小鼠可变剪接事件。
<strong>数据集17:人类RNA测序样本组的差异剪接分析:P值</strong>
本文件包含数据集15中汇总的人类可变剪接事件差异剪接分析的P值。文件格式、行名与列名均与数据集15相同。
<strong>数据集18:小鼠RNA测序样本组的差异剪接分析:P值</strong>
本文件包含数据集16中汇总的小鼠可变剪接事件差异剪接分析的P值。文件格式、行名与列名均与数据集15相同。
<strong>数据集19:小鼠RNA测序时间序列数据的转录本表达:估算读取计数</strong>
与数据集2一致,但针对本配套发表论文生成的时间序列数据。
<strong>数据集20:小鼠RNA测序时间序列数据的转录本表达:估算转录本丰度</strong>
与数据集5一致,但针对本配套发表论文生成的时间序列数据。
<strong>数据集21:小鼠RNA测序时间序列数据的可变剪接事件定量</strong>
与数据集14一致,但针对本配套发表论文生成的时间序列数据。
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Zenodo创建时间:
2019-01-15



