Labshake search
Citations for Illumina :
201 - 250 of 5074 citations for AS 1517499 CAS 919486 40 1 99% since 2020
Citations are collected from bioRxiv only, the total number of publications could be much larger.
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bioRxiv - Animal Behavior and Cognition 2021Quote: ... following manufacturer’s instructions (Illumina, San Diego, CA, USA), and assessed library quality prior to sequencing using a TapeStation 2200 (Agilent Technologies ...
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bioRxiv - Neuroscience 2021Quote: ... Small RNA sequencing using HiSeq2000 (Illumina Inc., CA) was performed by the Center for Genomic Science of IIT@SEMM.
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bioRxiv - Microbiology 2020Quote: ... TruSeq HT adapters (Illumina, San Diego CA, USA) were used to barcode the libraries ...
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bioRxiv - Genomics 2021Quote: ... Library sequencing was performed by Illumina HiSeq 2000 and MiSeq (Illumina, San Diego, CA) systems with read lengths of 93 nt or 101 nt (Seq 2000 ...
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bioRxiv - Cancer Biology 2020Quote: ... and Trusight Myeloid Panel (Illumina, San Diego, CA) with the exact same genetic regions of interest as the clinically utilized panel ...
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bioRxiv - Cell Biology 2021Quote: ... and sequenced on a NextSeq 500 (Illumina, CA) using 50 cycles single-end mode.
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bioRxiv - Genomics 2022Quote: ... Sequencing was performed by Illumina Novaseq 6000 sequencer (Illumina, San Diego, CA, USA) and NovaSeq 6000 S4 Reagent Kit v1.5 (200 cycles ...
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bioRxiv - Microbiology 2022Quote: ... lllumina MiSeq sequencing (Illumina, San Diego, CA, USA) was used to generate paired-end (PE ...
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bioRxiv - Cancer Biology 2020Quote: ... followed by the Nextera protocols (Illumina, CA, USA). Genome-wide expression profiles were obtained by sequencing of the samples on Illumina NextSeq 500 using NextSeq 500/550 High Output v2 kit.
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bioRxiv - Cancer Biology 2022Quote: ... using the bcl2fastq tool (Illumina, San Diego, CA).
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bioRxiv - Cancer Biology 2022Quote: ... using the bcl2fastq tool (Illumina, San Diego, CA). Germline variants found in the mesothelioma cohort (n = 122 ...
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bioRxiv - Immunology 2022Quote: ... The NovaSeq 6000 sequencer (Illumina, San Diego, CA) was used to sequence the amplified libraries on an SP flow cell of 28×10×10×90 to obtain approximately 50,000 reads per spot for each capture area covered by tissue ...
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bioRxiv - Microbiology 2020Quote: ... The Nextera XT Kit (Illumina, San Diego, CA) was used to prepare libraries ...
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bioRxiv - Genomics 2020Quote: ... TruSeq DNA Single indices (Illumina, San Diego, CA) were used instead of the EM-seq adaptor ...
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bioRxiv - Cancer Biology 2021Quote: ... and sequenced on a Nextseq500 (Illumina, CA, USA).
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bioRxiv - Genetics 2021Quote: ... TruSeq Stranded mRNA kit (Illumina, San Diego, CA) has been used for library preparation following the manufacturer’s instructions (library type ...
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bioRxiv - Genomics 2020Quote: ... 200 bp insert Illumina (Illumina, San Diego, CA) libraries were constructed and ligated with a unique index barcode ...
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bioRxiv - Microbiology 2021Quote: ... and MiSeq Reporter v2.6.2.3 software (Illumina Inc., CA). The sequences were analyzed by a pipeline of the 16s Microbiome Taxonomic Profiling of the EzBioCloud (https://www.ezbiocloud.net/ ...
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bioRxiv - Microbiology 2020Quote: ... following the manufacturer’s protocol (Illumina, San Diego, CA). Libraries were sequenced on the Illumina NovaSeq platform (2 × 150 bp ...
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bioRxiv - Genetics 2020Quote: ... A HiSeq 2000 instrument (Illumina, San Diego, CA) was used to sequence the genomic libraries ...
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bioRxiv - Genetics 2020Quote: ... in a HiSeq 2000 platform (Illumina Inc., CA). More than 30 M PE reads were obtained for all samples.
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bioRxiv - Molecular Biology 2023Quote: ... run on the HiScan System (Illumina, CA, USA) using manufacturer’s standard protocol.
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bioRxiv - Microbiology 2022Quote: ... The Nextera XT Kit (Illumina, San Diego, CA) was used to index the 16S rRNA PCR products as previously described [23] ...
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bioRxiv - Microbiology 2022Quote: ... The Nextera Flex kit (Illumina, San Diego, CA) was used to prepare the genomic library for MiSeq sequencing.
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bioRxiv - Neuroscience 2024Quote: ... The AmpliSeq protocol (Illumina, San Diego, CA, USA) was used in subsequent steps ...
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bioRxiv - Neuroscience 2023Quote: ... Libraries were sequenced on a NovaSeq6000 (Illumina, CA). Minimum 60M paired-end 2×150bp reads were generated per sample ...
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bioRxiv - Microbiology 2024Quote: Whole genome sequencing (Illumina, San Diego, CA, USA) was used to confirm the isolate identities and their phylogenetic relationships (Table 1 ...
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bioRxiv - Microbiology 2024Quote: ... with Illumina TruSeq adapters (Illumina, San Diego, CA) and a target insert size of 350 bp ...
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bioRxiv - Microbiology 2023Quote: ... a tag-encoded MiSeq-based (Illumina, CA, USA) high throughput sequencing was performed ...
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bioRxiv - Neuroscience 2023Quote: ... Illumina NovaSeq 6000 (Illumina, San Diego, CA, USA) was used to sequence the samples according to the manufacturer’s instructions using a 2×150bp Paired End (PE ...
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bioRxiv - Systems Biology 2024Quote: ... (Hongkong, China) on HiSeq platform (Illumina Inc., CA). Libraries were generated from 1 μg DNA per sample using the NEBNext Ultra DNA Library Prep Kit (NEB #E7645 ...
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bioRxiv - Microbiology 2023Quote: ... Illumina Novaseq 6000 (Illumina, San Diego, CA, USA) with 150 bp paired-end was performed.
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bioRxiv - Genomics 2022Quote: ... or a NOVA-seq (Illumina, San Diego, CA) according to the manufacturer’s instructions ...
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bioRxiv - Molecular Biology 2022Quote: ... The NextSeq HO Kit (Illumina Inc., CA, USA) with 150 cycles was used for paired end sequencing on the NextSeq 500 system (Illumina Inc. ...
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bioRxiv - Plant Biology 2022Quote: ... TruSeq stranded mRNA kit (Illumina, San Diego, CA) was used for library preparation and sequencing performed using Illumina NextSeq 500 platform (Illumina ...
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bioRxiv - Immunology 2022Quote: ... according to manufacturer instructions (Illumina, San Diego, CA). Amplicon sequences were quality filtered and classified using the UNOISE pipeline ...
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bioRxiv - Genomics 2022Quote: ... following manufacturer’s instructions (Illumina, San Diego, CA, USA).
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bioRxiv - Biochemistry 2023Quote: ... A NextSeq 500 sequencer (Illumina, San Diego, CA) was used to do paired-end deep sequencing (2X 150 bp ...
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bioRxiv - Genomics 2024Quote: ... paired end 2X150 kit (Illumina, San Diego, CA). The resulting raw sequence was only trimmed for adaptors ...
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bioRxiv - Microbiology 2024Quote: ... 2×150bp reads (20040534, Illumina, San Diego, CA). RNA sequencing was performed on a NovaSeq X Plus instrument ...
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bioRxiv - Immunology 2024Quote: ... according to manufacturer instructions (Illumina, San Diego, CA). Sequencing was performed using the V2 (150bp x 2 ...
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bioRxiv - Bioengineering 2024Quote: MiSeq Illumina sequencing (Illumina, San Diego, CA, USA) and data analysis were performed by Hokkaido System Science Co. ...
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Phenotypic and molecular evolution across 10,000 generations in laboratory budding yeast populationsbioRxiv - Evolutionary Biology 2020Quote: ... Libraries were sequenced to an average depth of 20-fold (haploids) or 40-fold (diploids) coverage using a Nextseq 500 (Illumina).
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bioRxiv - Molecular Biology 2021Quote: ... SmRNA libraries were prepared as described above using 800 ng of RNA containing 40 ng Drosophila melanogaster RNA as spike-in and sequenced with the Novaseq 6000 system (Illumina) to 40 – 90 million reads per sample.
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bioRxiv - Neuroscience 2023Quote: ... Paired-end strand-specific sequencing libraries were prepared from 40 ng total RNA using the TruSeq Stranded Total RNA Ribo-Zero Gold Library Preparation kit (Illumina). Following quality control on a BioAnalyzer (Agilent) ...
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bioRxiv - Cancer Biology 2023Quote: ... Each library was sequenced to a minimum of 40 million clusters or 80 million 150bp paired-end reads on a NovaSeq 6000 instrument (Illumina) at the University of Colorado Cancer Center Genomics Shared Resource.
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bioRxiv - Neuroscience 2023Quote: ... R2: 75) sequencing of approximately 40 million reads per sample using the High Output v2 kit (FC-404-2002, Illumina) on a NextSeq550 following the manufacturer’s instructions ...
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bioRxiv - Developmental Biology 2024Quote: ... Libraries were prepared at the UConn Center for Genome Innovation using the Illumina Strand mRNA Kit and 100bp paired-ends reads were sequenced to an average depth of 40 million reads/replicate on the NovaSeq (Illumina).
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bioRxiv - Cell Biology 2024Quote: ... Libraries were sequenced to a median depth of 35-40 million 100-bp single-end reads on a HiSeq sequencer (Illumina). The FASTQ files underwent quality control metrics (trimming) ...
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bioRxiv - Genomics 2024Quote: ... Pooled samples were sent to Admera Health and sequenced on a NovaSeq S4 (one pool with 40 samples) or NovaSeq X Plus (3 pools with 18-19 samples) platform (Illumina) using 150 bp paired-end reads.