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Citations for Illumina :
1 - 37 of 37 citations for Multi Analyte Recovery Spiking Std. 13C12 99% 200X Stock In Nonane since 2019
Citations are collected from bioRxiv only, the total number of publications could be much larger.
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bioRxiv - Developmental Biology 2024Quote: ... Sequencing was done using NovaSeq v1.5 STD (Illumina protocol #1000000106351 v03) for around 100,000 reads per cell ...
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bioRxiv - Microbiology 2020Quote: ... with a spiking of 20% PhiX control library (Illumina, San Diego, CA).
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bioRxiv - Microbiology 2022Quote: ... spiking with PhiX and sequencing with 2 x 250 bp paired-end reads with Illumina MiSeq (Illumina, San Diego, CA, USA).
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bioRxiv - Genetics 2023Quote: ... and aligned on GRCh37 by BlueFuse Multi software (Illumina) and CNVector tools (AB Vector) ...
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bioRxiv - Physiology 2023Quote: ... A second round of PCR was performed with 50 ng DNA input for 8 cycles to attach Nextera XT indices and adapters using the Illumina Nextera XT Index Kit (Illumina, Catalog #FC-131-200x) and Phusion HF PCR master mix (Thermo Fisher Scientific ...
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bioRxiv - Cell Biology 2023Quote: ... The BlueFuse Multi software (https://www.illumina.com/clinical/clinical_informatics/bluefuse.html) (Illumina) was used to generate karyograms ...
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bioRxiv - Genetics 2022Quote: ... and CNV calls were generated with BlueFuse Multi Software v4.2 (Illumina). CNV calls by SNP array were reported using standard clinical thresholds in the University of California San Francisco Clinical Cytogenetics Laboratory ...
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A rare variant on a common risk haplotype of HFE causes increased risk of hereditary hemochromatosisbioRxiv - Genetics 2019Quote: ... These individuals were genotyped with the Multi-Ethnic Global Array (Illumina) or the Infinium HumanExome BeadChip array (Illumina) ...
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bioRxiv - Systems Biology 2020Quote: ... The stocks were also validated by Illumina sequencing (see below).
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bioRxiv - Molecular Biology 2023Quote: ... Both cDNA and MULTI-seq-barcode libraries were sequenced with NextSeq500 (Illumina). We read 8 base pairs (bp ...
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bioRxiv - Microbiology 2022Quote: ... This seed stock was sequence verified by Illumina Next-Generation Sequencing to confirm the genome stability and avoid introduction of adventitious mutations and certified mycoplasma-free by PCR ...
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bioRxiv - Microbiology 2022Quote: ... The sequences of viral stocks were confirmed by Illumina HiSeq 2500 sequencing.
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bioRxiv - Genetics 2022Quote: Raw sequencing data were processed and visualized using Bluefuse Multi software (Illumina Inc, CA). A total of 30 samples (3.2% ...
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bioRxiv - Immunology 2021Quote: ... DNA was genotyped using the Illumina Global Screening Array v3.0+ multi disease bead chips (Illumina) and subjected to standard quality control filters ...
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bioRxiv - Genomics 2022Quote: Multi-omics data utilized in JHS analyses including methylomics (n = 1,750, Illumina MethylationEPIC BeadChip array) [40] and proteomics (n = 2,144 ...
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bioRxiv - Microbiology 2022Quote: ... SARS-CoV-2 stocks were deep sequenced on a MiSeq platform (Illumina). SARS-CoV-2 whole-genome amplicon-based sequencing was conducted by adapting an existing whole genome sequencing pipeline for poliovirus genotyping as described (Wang et al. ...
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bioRxiv - Immunology 2023Quote: ... The viral stocks were analyzed by qRT-PCR and sequenced by Illumina NGS to confirm the variant sequence and to ensure that no critical mutations had been selected for during the virus cultivation in cells ...
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bioRxiv - Microbiology 2021Quote: All SARS-CoV-2 stocks were deep sequenced on a MiSeq platform (Illumina).
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bioRxiv - Molecular Biology 2023Quote: ... 1μl of adaptors (1μl of a 1:250 dilution of Illumina stock solution), 2.5μl water and 1.5 ml of NEB Quick ligase (NEB ...
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bioRxiv - Microbiology 2023Quote: ... The genome sequences of all viruses were verified after stock production by Illumina sequencing ...
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bioRxiv - Developmental Biology 2021Quote: ... multi-cell sibling and bulk parental or grandparental DNA were genotyped on BovineHD BeadChips (Illumina, San Diego, California, US). Subsequently ...
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bioRxiv - Immunology 2021Quote: Virus stocks were sequenced using a MiniSeq platform (Illumina, Inc; San Diego, CA, USA). In brief ...
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bioRxiv - Genomics 2019Quote: ... we used the miRNA quantifications from all brain libraries with all starting amounts using both batches (total of 99 libraries, 19 for the Clontech, NEXTflex, Deduped and Fivepercent methods and 10 for Illumina and 13 for NEB). We normalized the data using the DESeq2(40 ...
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bioRxiv - Genetics 2020Quote: Genotyping was attempted on 6525 DNA samples using the Multi-Ethnic Genotyping Array (MEGA)V2 (EX) consortium chip on the Infinium iSelect platform by Illumina FastTrack Services (Illumina ...
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bioRxiv - Genomics 2020Quote: Peripheral blood DNA genotypes were obtained for 238 subjects using Infinium Multi-Ethnic Global-8 Kit (Illumina, San Diego, CA) and processed with GenomeStudio software ...
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bioRxiv - Microbiology 2020Quote: ... Samples were processed for WGS using multi-segment PCR [10] and then prepared for deep sequencing using the Nextera XT library preparation reagent (Illumina). Samples were sequenced on the Illumina NextSeq platform ...
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bioRxiv - Genomics 2022Quote: ... After purifying the Sample Tag PCR1 product indexing PCR was done following instructions of the MULTI-seq protocol where small RNA TrueSeq indexing primers (Illumina #15004197) were used for i7 and the Forward Primer from the BD WTA kit was used for i5.
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bioRxiv - Genetics 2023Quote: ... DNA extracts from the SAC individuals were genotyped for ∼1.6 million SNPs on the Illumina Multi-ethnic genotyping array (MEGA) (Illumina, Miami, USA).
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bioRxiv - Genetics 2022Quote: ... the genome FASTA file was augmented with ERCC sequences to create a STAR genome index with 99 bp overhangs (optimized for Illumina 2 × 100 bp paired-end reads). Two-pass mapping was executed ...
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bioRxiv - Genetics 2021Quote: Participants in the South African Zulu study were genotyped using the Illumina Multi-Ethnic Genotyping Array (Illumina, Illumina Way, San Diego, CA, USA). The Affymetrix Axiom PANAFR SNP array or Illumina Multi-Ethnic Genotyping Array was used to genotype participants in the AADM study ...
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bioRxiv - Genetics 2021Quote: Participants in the South African Zulu study were genotyped using the Illumina Multi-Ethnic Genotyping Array (Illumina, Illumina Way, San Diego, CA, USA). The Affymetrix Axiom PANAFR SNP array or Illumina Multi-Ethnic Genotyping Array was used to genotype participants in the AADM study ...
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bioRxiv - Genomics 2021Quote: ... We include QCed genotypes generated in the GCAT cohort with the Infinium Expanded Multi-Ethnic Genotyping Array (MEGAEx) (ILLUMINA, San Diego, California, USA) as described elsewhere18 (i.e ...
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bioRxiv - Pathology 2021Quote: ... The single nucleotide polymorphisms (SNPs) in BRSK2 gene region were genotyped by Infinium Asian Screening Array and Infinium Multi-Ethnic Global BeadChip (Illumina, Inc., San Diego, CA, USA), and SNPs passed through quality-control procedure (individual call rate >98% and approved with Hardy-Weinberg equilibrium ...
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bioRxiv - Immunology 2022Quote: Identity of virus stocks were confirmed by next-generation sequencing using a MiniSeq platform (Illumina, Inc; San Diego, CA, USA). RNA was purified from Trizol-inactivated material using a Direct-zol RNA Miniprep kit (Zymo Research ...
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bioRxiv - Microbiology 2022Quote: ... Passage 1 virus stocks were further produced in Vero TMPRSS2 cells and the presence of mutations was confirmed by Illumina sequencing ...
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bioRxiv - Microbiology 2022Quote: ... Genomic DNA was extracted from the final Δrv3645 RLC12 library stock and library quality was validated by deep sequencing (see Genomic DNA extraction and library preparation for Illumina sequencing).
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bioRxiv - Microbiology 2019Quote: ... PCR mixtures for amplification contained (per 25 µl reaction): 0.5 µl of each primer (515F and 806R with Illumina tags; 10 µM stock concentration), 12.5 µl of 2x KAPA HiFi Hotstart Readymix (Kapa Biosystems ...