Processed_qPCR_Data

Dryad2019-01-01 更新2026-04-13 收录

实时定量PCR数据分析

基因表达量化

数据链接：

https://datadryad.org/resource/doi:10.5061/dryad.b2r160s/4 数据链接链接失效反馈

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资源简介：

This file contains the information needed to normalize the Cq values from the raw data, as well as the final DCt values that were used in the manuscript.

创建时间：

2019-01-01

Assessment of potential chimerism in non-transgenic littermates and sows.

转基因动物嵌合体检测

实时定量PCR数据分析

ID, unique identification number; Ct, threshhold cycle in a quantitative real time PCR; ∞, no threshold cycle reached during PCR; n.d., not done; §, sow with two “transgenic” pregnancies.

NIAID Data Ecosystem50

Log2 fold changes of the four specifically amplified genes for validation resulting from the MACE analysis and RT-qPCR (calculated using REST with correction of amplification efficiencies).

基因表达验证

实时定量PCR数据分析

SE = standard error.Log2 fold changes of the four specifically amplified genes for validation resulting from the MACE analysis and RT-qPCR (calculated using REST with correction of amplification effic

Figshare2015-12-03 更新20

RNAseq is not required to determine stable reference genes for qPCR normalization

基因表达量化

参考基因稳定性分析

The original contributions presented in the study are included in the article & Supplementary Data. The metadata for the RNA-Seq and qPCR include the normalized count matrices for the RNAseq data,

Figshare2021-11-12 更新10

All_expressed_transcripts

转录组学分析

基因表达量化

The spreadsheet document contains all expressed transcripts in all genotype x treatment combinations in at least two out of in total three samples. Expressed values are presented in transcripts per mi

NIAID Data Ecosystem30

MOESM1 of Combined quantitation of HMGA2 mRNA, microRNAs, and mitochondrial-DNA content enables the identification and typing of thyroid tumors in fine-needle aspiration smears

甲状腺肿瘤分子诊断

基因表达量化

Additional file 1: Table S1. The oligonucleotide sequences used in the study.

Figshare2019-10-28 更新10