RNAseq and quantitative proteomic analysis of Dictyostelium knock-out cells lacking the core autophagy proteins ATG9 and/or ATG16

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RNAseq and quantitative proteomic analysis of Dictyostelium knock-out cells lacking the core autophagy proteins ATG9 and/or ATG16

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Autophagy is an evolutionary ancient mechanism that sequesters substrates for degradation within autolysosomes. The process is driven by many autophagy-related (ATG) proteins, including the core members ATG9 and ATG16. |

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RNAseq and quantitative proteomic analysis of Dictyostelium knock-out cells lacking the core autophagy proteins ATG9 and/or ATG16

Autophagy is an evolutionary ancient mechanism that sequesters substrates for degradation within autolysosomes. The process is driven by many autophagy-related (ATG) proteins, including the core members ATG9 and ATG16. |

Guide for library design and bias correction for large-scale transcriptome studies using highly multiplexed RNAseq methods

Cross-site comparison of ribosomal depletion kits for Illumina RNAseq library construction

Single-cell RNAseq for the study of isoforms—how is that possible?

RNAseq expression patterns of canine invasive urothelial carcinoma reveal two distinct tumor clusters and shared regions of dysregulation with human bladder tumors

Over-expression of Arabidopsis AtCHR23 chromatin remodeling ATPase results in increased variability of growth and gene expression

A deep survey of alternative splicing in grape reveals changes in the splicing machinery related to tissue, stress condition and genotype

Robust principal component analysis for accurate outlier sample detection in RNASeq data

SLFinder, a pipeline for the novel identification of splice-leader sequences: A good enough solution for a complex problem

GSEPD: A Bioconductor package for RNAseq gene set enrichment and projection display

Empirical assessment of the impact of sample number and read depth on RNASeq analysis workflow performance

Đang chuẩn bị liên kết để tải về tài liệu: RNAseq and quantitative proteomic analysis of Dictyostelium knock-out cells lacking the core autophagy proteins ATG9 and/or ATG16

Autophagy is an evolutionary ancient mechanism that sequesters substrates for degradation within autolysosomes. The process is driven by many autophagy-related (ATG) proteins, including the core members ATG9 and ATG16. |

Guide for library design and bias correction for large-scale transcriptome studies using highly multiplexed RNAseq methods

Cross-site comparison of ribosomal depletion kits for Illumina RNAseq library construction

Single-cell RNAseq for the study of isoforms—how is that possible?

RNAseq expression patterns of canine invasive urothelial carcinoma reveal two distinct tumor clusters and shared regions of dysregulation with human bladder tumors

Over-expression of Arabidopsis AtCHR23 chromatin remodeling ATPase results in increased variability of growth and gene expression

A deep survey of alternative splicing in grape reveals changes in the splicing machinery related to tissue, stress condition and genotype

Robust principal component analysis for accurate outlier sample detection in RNASeq data

SLFinder, a pipeline for the novel identification of splice-leader sequences: A good enough solution for a complex problem

GSEPD: A Bioconductor package for RNAseq gene set enrichment and projection display

Empirical assessment of the impact of sample number and read depth on RNASeq analysis workflow performance

Đang chuẩn bị liên kết để tải về tài liệu:
RNAseq and quantitative proteomic analysis of Dictyostelium knock-out cells lacking the core autophagy proteins ATG9 and/or ATG16