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Citations for Illumina :
201 - 250 of 9374 citations for Prostaglandin E2 PGE2 Multi Format ELISA Kit 1 Whole Plate since 2019
Citations are collected from bioRxiv only, the total number of publications could be much larger.
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bioRxiv - Evolutionary Biology 2023Quote: ... Library preparation and whole genome sequencing (using Illumina NovaSeq 6000) of 5 CRISPR mutants was performed by CeGaT (Tübingen ...
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bioRxiv - Microbiology 2023Quote: ... coupled with whole genome BAC sequencing (Illumina, San Diego, CA) verified that the insertion of vPOL-GFP and vPPF-GFP BACs did not lead to ORF coding changes or large-scale alterations of the viral genomes.
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bioRxiv - Microbiology 2023Quote: ... We performed whole-genome sequencing of the swaps by Illumina and used Breseq v0.36 [111] to verify off-target mutations (see Mutants and transconjugants validation) ...
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bioRxiv - Microbiology 2023Quote: ... and whole genome sequencing performed on a MiSeq instrument (Illumina) following the protocol provided by Illumina ...
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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 - Microbiology 2023Quote: ... The Seqwell plexWell LP384 Library Preparation Kit and Native Barcoding Kit 24 V14 (SQK-NBD112.24) were used for barcode-indexed whole genome sequencing with Illumina NovaSeq system (Illumina San Diego, USA) and Oxford Nanopore MinIoN Mk1C device (Oxford Nanopore Technologies ...
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bioRxiv - Microbiology 2023Quote: ... Whole-genome shotgun sequencing was carried out on an Illumina MiSeq platform using Nextera DNA Flex kits (Illumina, San Diego, CA, USA) with a 150-bp paired-end sequencing kit (Illumina ...
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bioRxiv - Cancer Biology 2022Quote: ... whole-genome and targeted libraries were added to flow cell in a 67%-33% ratio and sequenced to approximately 16M fragments per sample corresponding to ~1-2x whole genome coverage using NovaSeq S4 sequencing (Illumina) with 150 bp paired-end reads.
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bioRxiv - Immunology 2021Quote: ... Raw sequence data were obtained in Bcl-files and converted into fastq text format using the bcl2fastq program from Illumina. Validation of RNAseq was performed using qRT-PCR as described below.
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bioRxiv - Microbiology 2021Quote: ... Sequencing libraries were generated in 384-well format using a custom low-volume protocol based on the Nextera XT process (Illumina). Briefly ...
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bioRxiv - Immunology 2022Quote: ... Sequencing libraries were generated in 384-well format using a custom low-volume protocol based on the Nextera XT process (Illumina). Sequencing reads were generated using a NovaSeq S4 flow cell or a NextSeq High Output kit ...
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bioRxiv - Microbiology 2021Quote: Sequencing outputs were demultiplexed and converted to the fastq format for downstream analysis using the bcl2fastq (v2.19) conversion software (Illumina®). A total of 115,250,077 demultiplexed paired-end sequencing reads ...
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bioRxiv - Cell Biology 2020Quote: ... The pool of libraries was loaded onto one lane of an Illumina HiSeq 4000 flow cell and sequencing was performed in a 2 × 150 bp paired end format using HiSeq 4000 SBS reagents (Illumina) and approximately 312 million acceptable quality reads were achieved ...
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bioRxiv - Molecular Biology 2022Quote: ... Raw sequence data were obtained in Bcl-files and converted into fastq text format using the bcl2fastq program from Illumina. Mapping of transcripts was done using Genome UCSC annotation set for hg38 human genome assembly ...
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bioRxiv - Developmental Biology 2022Quote: ... Between 59M and 130M reads were sequenced per sample in a 100bp paired-end format using a NovaSeq 6000 (Illumina) platform ...
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bioRxiv - Microbiology 2022Quote: ... This pooled prep was subjected to PE 2x150bp format on the NextSeq2000 Illumina sequencing platform (Illumina, San Diego, CA, USA).
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bioRxiv - Genomics 2023Quote: ... The pooled libraries were sequenced in the 2 × 150bp format to an average depth of 300 million reads/sample on a NovaSeq 6000 S4 (Illumina) by Psomagen Inc.
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bioRxiv - Immunology 2024Quote: ... Raw sequence data were obtained in Bcl-files and converted into fastq text format using the bcl2fastq program from Illumina.
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bioRxiv - Genetics 2021Quote: ... homokaryotic mutants were crossed to a genetically polymorphic Mauriceville strain and approximately 15-20 antibiotic-resistant progeny were pooled and prepared for whole genome sequencing using the Nextera kit (Illumina, FC-121-1030). Mapping of the critical mutations was performed as previously described (Hunter 2007 ...
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bioRxiv - Microbiology 2021Quote: Whole genome sequencing libraries were prepared using either Nextera™ XT or Nextera™ DNA Flex library preparation kits (Illumina, Inc., CA, USA) following the manufacturers protocol ...
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bioRxiv - Microbiology 2022Quote: ... The extracted genomic DNAs were prepared for whole genome sequencing using the Nextera XT DNA library preparation kit (Illumina, San Diego, CA, USA) and sequenced on Hiseq and Miseq platform (Illumina ...
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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 - Plant Biology 2022Quote: ... were genotyped by using whole-genome sequencing (WGS) data from Illumina short-read sequencing with 3x genome coverage (Milner et al. ...
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bioRxiv - Evolutionary Biology 2020Quote: ... Sixteen aphid whole and partial mitochondrial genomes were assembled from Illumina Hiseq 4000 paired reads obtained from the Sequence Read Archive (SRA ...
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bioRxiv - Plant Biology 2022Quote: Whole Genome Sequencing was performed on the HiSeqX sequencing system (Illumina) by GeneWiz Inc. ...
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bioRxiv - Genetics 2023Quote: ... Then the whole genomes of the TAi strains were sequenced (Illumina).
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bioRxiv - Cancer Biology 2023Quote: ... Some whole-exome libraries were sequenced on a NovoseqPE150 sequencer (Illumina) to generate 12G of raw data per sample ...
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bioRxiv - Evolutionary Biology 2022Quote: ... whole genomes were sequenced using the HiSeq 2500 platform (Illumina, Inc) by the Genome Analysis Core Center located in the Petit Institute ...
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bioRxiv - Cancer Biology 2023Quote: ... whole tissue RNA-seq (Illumina NextSeq500 with paired-end 75bp reads) were performed on 4T1 orthotopically implanted mammary tumors in 8-12 week (young ...
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bioRxiv - Microbiology 2023Quote: All datasets in this study consist of whole genome sequences (Illumina) of Mtb strains collected in countries with a generalized HIV epidemic.
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bioRxiv - Genomics 2023Quote: ... Supplementary Table 2) was subjected to whole-genome sequencing by Illumina HiSeq ...
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bioRxiv - Evolutionary Biology 2023Quote: ... high-throughput genomic DNA library preparation and whole genome sequencing (Illumina HiSeq4000 ...
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bioRxiv - Microbiology 2024Quote: ... and whole genome sequencing was performed on the NextSeq platform (Illumina) with 2 x 150bp paired-end chemistry ...
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bioRxiv - Immunology 2019Quote: ... Basecall files (bclfiles) were demultiplexed and converted to fastQ file format using the bcl2fastq v2.18 software (Illumina Inc., San Diego, CA).
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bioRxiv - Cell Biology 2020Quote: ... The adapter-ligated library was completed by PCR with Illumina PE primers (8-11 cycles) and the resulting directional cDNA libraries were sequenced for 50 bases in a single-read format (Illumina HiSeq2000) and analyzed with nextpresso (Graña ...
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bioRxiv - Genomics 2020Quote: The raw data generated in binary base call (BCL) format from NovaSeq 6000 was processed using DRAGEN COVIDSeq Test Pipeline (Illumina Inc.) on the Illumina DRAGEN v3.6 Bio-IT platform as per standard protocol ...
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bioRxiv - Genetics 2021Quote: ... including a whole-genome sequencing (WGS) data set of 1196 subjects in the VCF format and two SNP array data sets of 382 (Illumina HumanOmniExpress) and 1709 (Affymetrix GeneChip 6.0 ...
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bioRxiv - Genomics 2023Quote: ... These BAM files were quality checked by using systemPipeR’s alignStats function and subsequently a gene reads table was calculated by the summarzieOverlaps function of the GenomicAlignments (29) R/BioConductor package and the corresponding Gene Transfer Format (GTF) file (Illumina’s iGenomes). Normalization and detection of deregulated genes was performed using the DESeq2 v ...
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bioRxiv - Microbiology 2023Quote: ... Genomic DNA libraries were prepared for whole genome sequencing using the Tagmentation-based library prep kit according to the manufacturer’s instructions (Illumina Inc, San Diego, CA, USA). Next ...
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bioRxiv - Cell Biology 2020Quote: ... and hybridized on Illumina whole-genome HumanHT-12 v 4.0 chip (Illumina). Acquisition and data analysis were performed as previously described14 ...
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bioRxiv - Cancer Biology 2021Quote: ... Whole genome DNA methylation profiling was done on Infinium HumanMethylation450 BeadChip (Illumina) and signal intensity on bead chips were converted to raw data using the iScan platform (Illumina) ...
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bioRxiv - Cell Biology 2021Quote: Whole-genome genotyping was performed using the Illumina HumanOmni1-Quad Beadchip (Illumina) containing 1,140,419 genetic markers across the human genome ...
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bioRxiv - Microbiology 2022Quote: ... We sequenced the whole genome of these isolates using shorts reads (Illumina) combined with long reads [Oxford Nanopore Technologies (ONT)] sequencing techniques to generate de novo assembled genomes for each of them.
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bioRxiv - Genetics 2022Quote: ... Whole genome sequencing was performed on HiSeqX or NovaSeq 6000 Systems (Illumina) using paired-end sequencing method (2×150bp ...
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bioRxiv - Microbiology 2022Quote: ... Whole genome sequencing was performed using a NextSeq 500 system (Illumina, USA) at the Mutualized Platform for Microbiology of Institut Pasteur ...
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bioRxiv - Genomics 2022Quote: ... including Illumina whole genome shotgun sequencing (150 bp PE, Illumina HiSeq X) augmented with Dovetail’s complementary Chicago (relying on artificial chromatin constructed in vitro ...
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bioRxiv - Genomics 2019Quote: ... nine whole-genome datasets from Japanese lung cancer patients (150PE, Illumina NovaSeq), 514 whole-exome datasets from TCGA-LUAD and 97 whole-exome datasets from Japanese lung adenocarcinoma patients (JGAS00000000001 ...
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bioRxiv - Genomics 2019Quote: ... 5 whole-genome datasets from cancer cell lines (DRA001859; 101PE, Illumina HiSeq2500), nine whole-genome datasets from Japanese lung cancer patients (150PE ...
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bioRxiv - Genomics 2020Quote: We screened a large collection of publicly available whole genome sequences (Illumina) of MTBC strains belonging to L1 and L3 ...