Hi,
I am currently working on GAII. hoping to learn from y'all!
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Hi,
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Hi. I'm the bioinformatics guy/sysadmin/programmer in our lab. We're studying metagenomics, which means tons of sequence data. Yaaaay!
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Hi
Hi, just getting into resequencing and found SEQanswers quite helpful, so I wanted to signup.
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Introduction
Hi. I'm one of the developers of the Savant Genome Browser. If anybody has questions or comments about Savant, feel free to contact me.
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Hey-
I am new member, and began working with the 454 GS Junior the last year. I am a technician here in Athens, GA. I do all the benchwork and upkeep with the Jr, but hope to do some analysis soon. I think this forum is very useful and I decided to join. I have done shotgun libraries for the large FLX and now do rapid libraries and some paired end runs on the Jr. Hope to do more studies soon.
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Hi all,
I am an application specialist. I have Bachelor of Science in Biomedical Engineering and 2nd Major in Pure Mathematics for curiosity reasons. I havn't found direct benefit of it but I might be wrong. I am my own mentor for the good and bad. I am involved in developing highthroughput screening projects since 2006. strong practical experience in linux being mathematically inclined. my dad bought me a computer in early 80's when I was less than 10 years old. I remember it had MSX, enough said about me.Last edited by husamia; 06-30-2011, 06:16 AM.
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Hi all,
I'm a PhD student in a plant genetics lab. Being a linux user with some programming experience, I seem to have become the "bioinformatics guy" in the lab. We've already successfully used SHORE to identify two mutants from a mutagenesis via resequencing; now I'm trying to prepare to analyse some RNAseq data from one of our mutants.
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Hello
Hi, I'm a lab tech who's recently been told I'll be doing all of our 454 analysis work. Figured this place as well as other faqs and everything else would be a good resource. Will probably post my first question very soon. (and I used to think I was alright with computers)
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Hello, I am a grad student from Michigan State working on plant-associated metagenomes and evo genomic analysis of a plant pathogen. Thanks for all the helpful comments here!
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Originally posted by aeonsim View PostHi
I'm an Analyst working for a Animal Breeding company in NZ. We're just starting a WGS using the Illumina Hiseq platform and had our first lot of data arrive (300+ coverages split among a number of animals). My focus at the moment is getting my head around how we are going to deal with all the data, comparing the various tools and assembling a decent pipeline for SNP calling.
My background is in Biochemistry.
Wes Barris and Brian Dalrymple at the CSIRO are experts in this field. Brian maybe sympathetic as he is a Kiwi (as am I)
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Hello from Sci_guy
Hi,
My name is Jason and I work in Sydney for the CSIRO. I was a molecular biologist but now I've gone to the dark side and exchanged my pipettes for a Linux shell. I've been involved with mostly epigenomics deep seq projects which have needed a fair amount of bioinformatics crowbar work. I spend my days writing R/Python/Perl/SQL.
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Originally posted by aeonsim View PostHi
I'm an Analyst working for a Animal Breeding company in NZ. We're just starting a WGS using the Illumina Hiseq platform and had our first lot of data arrive (300+ coverages split among a number of animals). My focus at the moment is getting my head around how we are going to deal with all the data, comparing the various tools and assembling a decent pipeline for SNP calling.
My background is in Biochemistry.
Could you please give your email address. SNP calling progress is a little complex, I think we can exchange our experience by email.I collected some papers, maybe could help you.
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Hi
I'm an Analyst working for a Animal Breeding company in NZ. We're just starting a WGS using the Illumina Hiseq platform and had our first lot of data arrive (300+ coverages split among a number of animals). My focus at the moment is getting my head around how we are going to deal with all the data, comparing the various tools and assembling a decent pipeline for SNP calling.
My background is in Biochemistry.
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fcmChIP
Hi folks,
I am a staff scientist with the FDA, but on the NIH campus in Bethesda, MD.Research interest is in antibody locus control regions and isotype switching. My experience is in chromatin and molecular immunology, including ChIP. I would characterize by bioinfo experience as lengthy, but at a relatively low level: MacVector for many years, and also UCSC browser. Also some programming experience. Looking to do more sophisticated mining of ENCODE data, and our center is getting an Illumina-it would be nice to be able to analyze ChIP Seq data at least at the level of peak calling.
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by seqadmin
The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist...-
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04-22-2024, 07:01 AM -
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by seqadmin
Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...-
Channel: Articles
04-04-2024, 04:25 PM -
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