sys4seq's profile picture. Systems Biology for Sequencing #startup (Sys4Seq), #DataScience, #Bioinformatics, #NGS, #themicrobiome, #GWAS, #RareDisease, #CloudComputing

Sys4Seq, LLC

@sys4seq

Systems Biology for Sequencing #startup (Sys4Seq), #DataScience, #Bioinformatics, #NGS, #themicrobiome, #GWAS, #RareDisease, #CloudComputing

Sys4Seq, LLC hat repostet

This is an outstanding study, and thread. One of the best virology manuscripts on B117.

Very excited to tell you all about our new PRE-PRINT biorxiv.org/cgi/content/sh… - Altered subgenomic RNA expression profiles in B.1.1.7 #SARSCoV2 using @nanopore & @NetworkArtic genomic seq data. This builds on our previous work describing sgRNA detection using this data 1/10

bioinfomatt's tweet image. Very excited to tell you all about our new PRE-PRINT biorxiv.org/cgi/content/sh… - Altered subgenomic RNA expression profiles in B.1.1.7 #SARSCoV2 using @nanopore & @NetworkArtic genomic seq data. This builds on our previous work describing sgRNA detection using this data 1/10


Sys4Seq, LLC hat repostet

Ready to test your genetics knowledge again? Answer this week's poll question below! Approximately how many rare diseases currently exist?


Sys4Seq, LLC hat repostet

“Except for polio, which is transmitted only from human to human, most of those disease agents were part of natural cycles that involved only animals. They spilled over into humans because nature was disturbed in some way. There is a lesson in that.” apple.news/AMIgHUHyaTS6iL…


Sys4Seq, LLC hat repostet

Tumor-specific splicing alterations are created by mutations that disrupt splicing-regulatory elements within genes and impair splicing recognition or by altering the RNA-binding preferences of individual splicing factors. sciencedirect.com/science/articl…


Sys4Seq, LLC hat repostet

Parents and caregivers of little ones, please watch. Cases of RSV are on the rise. If you see labored breathing that looks like this, contact your child’s doctor immediately. RSV can be more than a cold, and knowing the warning signs can be lifesaving.


Sys4Seq, LLC hat repostet

Impact of Th1 CD4 TFH skewing on Antibody Responses to an HIV-1 Vaccine in Rhesus Macaques jvi.asm.org/content/early/… #systemsvaccinology #HIV #transcriptome


Sys4Seq, LLC hat repostet

Rectal Microbiome Composition Correlates with Humoral Immunity to HIV-1 in Vaccinated Rhesus Macaques msphere.asm.org/content/4/6/e0… #systemsvaccinology #HIV #microbiome


Sys4Seq, LLC hat repostet

EdgeR for differential expression is included but not DESeq2!!

Bioconda, Matplotlib, Scipy, Open Refine, BWA, Qiime2 and more that are used regularly. Fantastic to have a support for #Opensource tools. A lot of good software die soon because of no support to keep them working. #OpenSource #Reproducibility



Sys4Seq, LLC hat repostet

There are existing standards for the analysis of common variants in genome wide studies. However, inferring the role of rare variants in disease poses many challenges that require new approaches and standards. Excellent @NatureRevGenet review. nature.com/articles/s4157…

MuinJKhoury's tweet image. There are existing standards for the analysis of common variants in genome wide studies.  However, inferring the role of rare variants in disease poses many challenges that require new approaches and standards.  Excellent @NatureRevGenet review. nature.com/articles/s4157…
MuinJKhoury's tweet image. There are existing standards for the analysis of common variants in genome wide studies.  However, inferring the role of rare variants in disease poses many challenges that require new approaches and standards.  Excellent @NatureRevGenet review. nature.com/articles/s4157…

Sys4Seq, LLC hat repostet

A small set of fast Rust scripts to convert various single cell output matrix formats [h5, csv, mtx, eds] into each other. github.com/COMBINE-lab/EDS

k3yavi's tweet image. A small set of fast Rust scripts to convert various single cell output matrix formats [h5, csv, mtx, eds] into each other. github.com/COMBINE-lab/EDS

Sys4Seq, LLC hat repostet

MapCaller - An integrated and efficient tool for short-read mapping and variant calling using high-throughput sequenced data biorxiv.org/content/10.110… github.com/hsinnan75/MapC…

strnr's tweet image. MapCaller - An integrated and efficient tool for short-read mapping and variant calling using high-throughput sequenced data biorxiv.org/content/10.110…
github.com/hsinnan75/MapC…
strnr's tweet image. MapCaller - An integrated and efficient tool for short-read mapping and variant calling using high-throughput sequenced data biorxiv.org/content/10.110…
github.com/hsinnan75/MapC…

Sys4Seq, LLC hat repostet

Stool sampling and DNA isolation kits affect DNA quality and bacterial composition following 16S rRNA gene sequencing using MiSeq Illumina platform - ow.ly/iHyp30pBFFq


Sys4Seq, LLC hat repostet

STILL DON'T KNOW how to plan your #SingleCell transcriptome experiment? READ HERE OUR TUTORIAL: Guidelines for the experimental design of single-cell RNA sequencing studies @NatureProtocols. nature.com/articles/s4159…


Sys4Seq, LLC hat repostet

A step by step explanation of Principal Component Analysis towardsdatascience.com/a-step-by-step…


FutureNeuro researchers integrate genomics data in to electronic patient records - SCIENMAG apple.news/AyoGUQzsGTHmms…


Sys4Seq, LLC hat repostet

I am going to keep bringing up this plea as long as people keep using Tophat. This recently published paper used TopHat 1.4.1: stm.sciencemag.org/content/11/478…

Please stop using Tophat scholar.google.com.mx/scholar?hl=es&… Cole and I developed the method in *2008*. It was greatly improved in TopHat2 then HISAT & HISAT2. There is no reason to use it anymore. I have been saying this for years yet it has more citations this year than last #methodsmatter



Sys4Seq, LLC hat repostet

A nice read on estimating true number of cells in scRNAseq cgatoxford.wordpress.com/2017/05/18/est… #scRNAseq


Loading...

Something went wrong.


Something went wrong.