Primers used for quantitative reverse transcription PCR.

NIAID Data Ecosystem2026-03-08 收录

PCR引物

基因表达分析

数据链接：

https://figshare.com/articles/dataset/_Primers_used_for_quantitative_reverse_transcription_PCR_/1429362 数据链接链接失效反馈

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资源简介：

Primers used for quantitative reverse transcription PCR.

创建时间：

2015-05-28

Petrolisthes cinctipes Transcriptome or Gene expression. Petrolisthes cinctipes

甲壳类转录组

基因表达分析

Transcriptome of the flat porcelain crab, Petrolisthes cinctipes, collected from the Sonoma Coast of Northern California, near Fort Ross. Assembly made using Trinity from RNA-seq library 100bp paired

NIAID Data Ecosystem40

Additional file 6 of Super-delta: a new differential gene expression analysis procedure with robust data normalization

基因表达分析

数据归一化

Rank difference analysis. This file contains information of most differently ranked significant genes between super-delta and quantile normalization. (XLSX 852 kb)

DataCite Commons2024-03-25 更新40

mRNA_PSE_18C_F3_2.fastq.gz

转录组测序

基因表达分析

RNA-seq fastq file for sample PSE_18C_F3 (pair-end 2).

DataCite Commons2026-03-13 更新00

Comprehensive Evaluation of AmpliSeq Transcriptome, a Novel Targeted Whole Transcriptome RNA Sequencing Methodology for Global Gene Expression Analysis.

基因表达分析

RNA测序方法评估

Background: Whole transcriptome sequencing (RNA-seq) represents a powerful approach for whole transcriptome gene expression analysis. However, RNA-seq carries a few limitations, e.g., the requirement

NIAID Data Ecosystem40

Next Generation Sequencing analysis of VL and VH regions following PCR #2 using standard or rh-PCR primers.

抗体库测序

PCR引物

Amplicons for NGS were prepared following cloning of PCR fragments into mammalian expression vectors as outlined in Fig 8A. The average number of full-length reads was determined based on the percenta

NIAID Data Ecosystem30

Primers used for quantitative reverse transcription PCR.

资源简介：

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