Hello,
I am doing a comparison of duplicated reads on Illumina NovaSeq vs MGI G400 by checking the distribution of reads on the flowcell....
17 results in 0.0027 seconds.
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G400 fastq header description?
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Complete Genomics: Spotlight on the Companies Shaping Genetic Research
After celebrating its 18th birthday, the team at Complete Genomics is more committed than ever to providing the sequencing community with affordable sequencing solutions. It comes as no surprise as their Co-founder and Chief Scientific Officer Dr. Radoje (Rade) Drmanac has a long history of paving the way for the advancement of genomics. From working on the Human Genome Project to his various genomic startups, Drmanac has always had the goal of improving genomics research and technologi... -
DNBSEQ-G400 from Complete Genomics: Latest Sequencing Technologies—Part 5
Complete Genomics (an MGI company) released the DNBSEQ-G400 into the U.S. market this summer. DNBSEQ-G400 is a benchtop sequencer that uses MGI’S DNA Nanoball sequencing technology (DNBSEQ) that boasts low index hopping, low amplification bias, and low PCR amplification error accumulation. In addition, the instrument is capable of using an improved antibody-based chemistry, CoolMPS sequencing reagent, that reduces errors and improves the sequencing quality.
Read type and length... -
No coverage or very low coverage in the Complete Genomics data
Hi,
Has anyone worked on Complete Genomics data? Most of the exons in the data have no coverage or very low coverage (5-10 reads only)... -
Complete genomics data analysis, pipeline version differences and batch efffect
I am working with Complete genomics data from pipeline version 2.5. I need to add 1000 genome data to my sample and make a multigenome vcf file. Since... -
BGI / Complete Genomics / File conversion cgatools
Hello,
I few weeks ago I received the results of my Exome sequencing project.
Can someone help me with the conversion to... -
CNV and SV analysis of Complete Genomics data
Any suggestions for tools/pipelines to identify CNVs and SVs from Complete Genomics data? Anyone with any experience doing this?
Has anyone... -
Complete Genomics CNVs and SVs
Any suggestions for tools/pipelines to identify CNVs and SVs from Complete Genomics data? Anyone with any experience doing this?
Has anyone... -
Are public CG reads SE reads or PE reads?
I was runningon the file ftp://ftp2.completegenomics.com/YRI_trio/MAP_Build37_2.0.0/NA19240/NA19240-L2-200-37-MAP/GS27651-FS3-L01/reads_GS2...Code:head -20
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Inconsistencies between evidence and SAM files
Hi everyone,
The evidence2sam command which produces the SAM file, contains records/lines where a every read is repeated twice mapping... -
samtools: bam_pileup.c:112: resolve_cigar2: Assertion `s->k < c->n_cigar' failed
Hi,
I have a bam file that I have run through the GATK pipeline (i.e. de novo realignments around indels, duplicates removed and quality... -
RTG Investigator 2.3.2: Improved Ion Torrent, lower RAM usage
We're pleased to announce the latest version of RTG Investigator.
Highlights include:
* Improved Ion Torrent support... -
How to generate de novo assembly sequence from complete genomics data?
Hi, all,
recently we got a few samples' sequence data from complete genomics, we hope to generate a de novo assembly sequence. But i didn't find...Last edited by ssnowfox; 09-27-2011, 09:11 AM. -
Announcing Complete Genomics Cancer Grant Program
As the use of DNA sequencing data in cancer research has become widespread, significant progress is being made with respect to characterization of a variety... -
Hi
Hi
I work at Complete Genomics in the Customer Support Department.
I'll be poking around the forums, trying to address any...
