118 results in 0.0048 seconds.
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Consortium Completes First Full Diploid Human Genome
Scientists have reconstructed the complete genome of a real person, including full sets of chromosomes from each parent, an achievement expected to advance... -
UC San Diego Bioengineers Map Gene Function in Human Stem Cells
Bioengineers at the University of California San Diego have developed a genome-scale reference map showing how individual genes control the functions...Last edited by SEQadmin2; 08-03-2026, 10:12 AM. -
SEQadmin2 started a topic International Team Sequences the Genomes of Indigenous Peoples Across the Americasin NewsInternational Team Sequences the Genomes of Indigenous Peoples Across the Americas
An international research team has sequenced the largest genomic dataset yet assembled for Indigenous peoples of the Americas, generating 199 genomes... -
Bcftools installed via Cygwin plugin error
Hi! I am trying to look at several genomes of different individuals of the same species and call the SNPs for each genome using bcftools. I installed... -
What is the file .mums created by mummer ?
Hello !
I am doing genome sequence alignment using MUMmer, in particular I want to do a dotplot with mummerplot. So the passages that I... -
Viral Genome reconstruction
Hi! I have some reads from sequencing a viral genome. We are analyzing readings with two matches, and we calculate the existing distance between both... -
Analyzing PacBio sequel data and SRA
I am new to NCBI's SRA and pacbio sequencing data analysis. I am trying to download pacbio sequence data from SRA and my goal is get CCS (Consensus) reads... -
Any user friendly way to find rare mutations in whole genome raw?
Is there any user friendly way to find rare mutations in the individual human whole genome sequencing raw data? (from Dante, 30x coverage).
...Last edited by Larendy; 01-07-2020, 03:38 PM. -
Scaffolding with reads from other individuals
I'm currently woking on the assembly of a diploid eukaryotic genome using a combination of PacBio Sequel subreads and Illumina NextSeq paired-end reads...Last edited by adamrork; 01-03-2020, 09:28 PM. -
CRISPR Genome Editing course in Berlin
Dear all,
Still places left on our 3-day course "Approaches and Computational tools for CRISPR Genome editing", which is being... -
What's the exact pathway to handle paired end fastq data so you finally make it into
I've unmapped cleaned paired end sequence data in fastq format of a bacterial genome. I want to get a sequence data in Genbank format in the end. What's... -
How to add GFP sequence to mouse genome for mapping
Hi guys,
I was wandering what is the right way to add the sequence of GFP reporter to a mouse genom. Basically instead of "geneA" in... -
suitable aligner for human RNA-seq
Hello,
Human RNA-seq dataset was generated from Illumina HiSeq 3000 with 2X100 cycles run.
The first step is making alignment... -
best suitable aligner for RNA-seq mapping
Hello,
Human RNA-seq dataset was generated from Illumina HiSeq 3000 with 2X100 cycles run.
The first step is making alignment... -
help to do genome assembly
I prepare genomic shotgun libraries for sequencing using Single Molecule Real Time (SMRT) sequencing platform produced by PacBio (20X coverage of PacBio...
