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Biology版 - Any suggestion about RNA-seq?
相关主题
Kit for libary construction for next-generatin sequenceRe: about RNA
请问NGS illumina的几个概念how to analyze microRNA and mRNA microarray data set together?
knockdown efficiency 为何microarray和qPCR测出来不同?蛋白表达量与microarray及real time PCR所测得的mRNA改变不一致怎么办?
microarray 统计问题有做过转录因子knockdown后用Microarray看target gene的吗?
请教RNA-seq 软件的安装调试的问题!microarray intron probe
求解RNA-seq求助!
那个构建RNA Seq library的kit 最好用Re: questions about the latest version of human genome
mRNA降解是从5'端开始还是3’端开始还是从中间开始的?Re: 请推荐个提mRNA的kit吧
相关话题的讨论汇总
话题: rna话题: lane话题: seq话题: some话题: any
进入Biology版参与讨论
1 (共1页)
H*****e
发帖数: 120
1
Hi,
I have some samples that I prepared for microarray. When I went to the core
, I noticed that the core has only a few people do array now but most of
them do RNA-seq. They pass me some information like I know everything. But
, after read them for the whole morning, I still no idea what to do.
Especially,
1. Library: What is the difference and advantage between Single Read and
Paired end and mRNA and small RNA libraries.
2. Lane: some run one lane and some run 1/2 lane.
3. Cycle numbers: h
d***y
发帖数: 8536
2
1 Paired end is much better than single end.
2 Normally,1 lane is necessary. About 1/2 lane, I think they mix your sample
with other sample in the one lane?
3 I don't know the cycle numbers. You could call customer service of the
sequence company.
Good luck.
1 (共1页)
进入Biology版参与讨论
相关主题
Re: 请推荐个提mRNA的kit吧请教RNA-seq 软件的安装调试的问题!
Good stuff, not too late求解
能用real time RT-PCR来比较同一细胞的不同gene的含量吗?那个构建RNA Seq library的kit 最好用
哪些基因RNA表达变化,蛋白却无明显相应变化?mRNA降解是从5'端开始还是3’端开始还是从中间开始的?
Kit for libary construction for next-generatin sequenceRe: about RNA
请问NGS illumina的几个概念how to analyze microRNA and mRNA microarray data set together?
knockdown efficiency 为何microarray和qPCR测出来不同?蛋白表达量与microarray及real time PCR所测得的mRNA改变不一致怎么办?
microarray 统计问题有做过转录因子knockdown后用Microarray看target gene的吗?
相关话题的讨论汇总
话题: rna话题: lane话题: seq话题: some话题: any