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Hi everyone! I'm a junior faculty at UCSF and I am keen to use ChIP and deep sequencing to address questions of mechanisms of transcriptional regulation during development.
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Hello
Hi, everyone. My name Ximiao He. I am from China, and now doing my post-doctoral research at NCI, NIH. And now, I am doing analysis of Bisulfite Sequencing data using Illumina, also the ChIP-seq and RNA-seq data.
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hello
I am Yuliang. I work in Univ of Illinois, Urbana-Champaign. My lab mainly focuses on networks, but also began to do RNA-seq. I learned a lot in this community. Thanks to everyone
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Keley Nunes
Hi, everybody !
I´m Biologist , working at a brazilian federal institution named Evandro Chagas Institute, located in Pará State. I´m looking for someone who has experienced RNA virus sequencing in SOLID plataform to share with us. Actually we are facing problems to deal with RNA sequencing, even before to get it into the plataform, I mean , dealing with the library preparation.
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Hello everybody,
I am Chaithra, doing my PhD in UK and would be dealing with RNASeq analysis. I am glad I found a place to clear my doubts!!!
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Hello
Hi, I am Gianni! I am doing my PhD and I just started to deal (with some difficulties) with sequencing technologies. I find it great
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Hi! I am Gianni. I am doing my PhD in Germany and I am just starting (with some difficulties) to deal with sequencing technologies. I find it great!
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Warm Greetings Folks!
I am Maharajah (Maha) Post Doc in CNG (National Centre for Genotyping) in Evry, Paris. I am working on Whole Genome Resequencing using Illumina...and SNP mining..
Very Glad to be a part of this wonderful Community..!!!
Cheers..
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Hi!
Hi Everybody,
I am a Ph.D. student in Colorado, USA working on a thesis involving colony variation of a pathogenic bacteria (and how it relates to disease). I am not using a Next-Gen sequencing machine myself, however I am in the process of analyzing next-gen sequencing data from some of my variants to see if we can uncover some explanations for why the variants behave as they do.
I've been mucking around a little bit with various pieces of software and recently got GenomeStudio (DNA sequence analysis module) up and running and I am very excited to have a place I can come ask questions (some of that Linux stuff is incredibly intimidating!)
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Hi,
I'm master student in bioinformatics in Geneva with bioinformatics background (yes always been one
). I'm from Montreal
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Hi everybody,
I'm a student of the undergraduate program "bioinformatics" in Frankfurt, Germany. Currently I'm preparing my thesis, which will be on transcriptome assembly and analysis. So I'm very interested in algorithms, technical issues and workflows to handle big datasets as well as sequencing technologies and their data formats. Thanks to everyone who provides help to newbies here :-)
Yours Jenzo
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Dear all,
I'm a biologist and bioinformatician. I'm beginning a Post-Doc in INRA (French National Institute for Agricultural Research) near Paris. The NGS experiments I'll work on deal with host/pathogen interactions in swine model.
cheers
Marie-Laure
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Dear all --
I'm a theoretical biologist by training with a focus mainly on Biodiversity and Phylogenetics. My fields of activity cover the handling & processing of large quantities of data (fresh starting with data from NGS/pyrosequencing) alike the planning of an adequate IT-Infrastructure to accomplish this task.
Cheers,
Claus.
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Baby NGS data analyst
Hi all, I'm a baby NGS data analyst and hope to grow quickly, get up and running as soon as possible with this community.
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Hi,
I am a biotechnologist who now works as bioinformatician/researcher. I am Polish, but I live in Wageningen, Netherlands.
Greetings to everyone,
A.S.C.
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by SEQadmin2
CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).
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Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.
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by SEQadmin2
Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
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