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Citations for Illumina :
51 - 100 of 272 citations for Hepatitis B Virus Core Antigen HBcAg since 2019
Citations are collected from bioRxiv only, the total number of publications could be much larger.
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bioRxiv - Physiology 2021Quote: ... Libraries were generated by the Genomic Technologies Core Facility using the TruSeq® Stranded mRNA assay (Illumina, Inc.) according to the manufacturer’s protocol ...
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bioRxiv - Evolutionary Biology 2020Quote: ... and converted to cDNA) was sequenced in CEITEC MU Genomics Core Facility on a NextSeq500 platform (Illumina®) using NextSeq 500 v2.5. ...
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bioRxiv - Genetics 2021Quote: ... Sequences were demultiplexed using QIIME2 (core distribution 2018.6)42 for dataset 1 and BCL2FASTQ (Illumina, San Deigo, CA) for dataset 2 ...
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bioRxiv - Evolutionary Biology 2022Quote: ... Libraries were transported to the Cancer Research UK Genomics Core Facility and sequenced on NovaSeq 6000 system (Illumina).
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bioRxiv - Biophysics 2023Quote: ... at the UNMC Sequencing core using miSeq reagent kit v3 (600 cycles) 2 x 300 read length (Illumina). The total number of reads were 1-2 million reads per sample.
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bioRxiv - Microbiology 2024Quote: ... RNA was submitted to the University of Michigan Advanced Genomics Core for library preparation and RNA-sequencing (Illumina NovaSeq platform ...
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bioRxiv - Zoology 2020Quote: ... but with TruSeq DNA Single Indexes (Set B, Illumina), following the manufacturers’ instructions up till the adapter ligation step ...
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bioRxiv - Systems Biology 2019Quote: ... Set B: indexes 13–24 (Illumina, RS-200-0024), Set C ...
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bioRxiv - Cell Biology 2020Quote: ... and TruSeq RNA Single Indexes Set B (20020493, Illumina) according to standard Illumina library preparation procedure ...
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bioRxiv - Microbiology 2020Quote: ... The virus was passaged three times in VeroE6 cells and genotype sequence confirmed by Illumina sequencing ...
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bioRxiv - Molecular Biology 2021Quote: ... Libraries were multiplexed and sequenced at the University of Massachusetts Amherst Genomics Core Facility on the NextSeq 500 (Illumina). Single nucleotide polymorphisms (SNPs ...
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bioRxiv - Microbiology 2022Quote: ... cDNA libraries were prepared by the University of Michigan DNA Sequencing Core using the TruSeq Stranded mRNA Kit (Illumina) according to the manufacturer’s protocol ...
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bioRxiv - Developmental Biology 2021Quote: ... Library preparation and Illumina sequencing were performed at the École Normale Supérieure genomics core facility (Paris, France) on a NextSeq 500 (Illumina). Three replicates were sequenced for each genotype ...
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bioRxiv - Genetics 2019Quote: ... Libraries for Illumina sequencing were prepared at the IBBR sequencing core as per manufacturer’s instructions and sequenced using a HiSeq1000 (Illumina).
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bioRxiv - Microbiology 2019Quote: ... and submitted to The University of Chicago Genomics core for library preparation and sequencing on a HiSeq4000 platform (Illumina). Reads were mapped to a concatenated version of the human and HSV-1 genomes with STAR aligner (see single-cell RNA-sequencing above for details) ...
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bioRxiv - Genomics 2021Quote: ... according to the manufacturer’s protocol and sequenced at the CCHMC Core Facility using Illumina HiSeq 2500 sequencing system (Illumina) to generate 100 bp paired-end reads ...
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bioRxiv - Neuroscience 2022Quote: ... Next-generation sequencing (VIB Nucleomics Core) of the single-cell libraries was carried out on a NovaSeq 6000 (Illumina) platform with the following read configuration ...
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bioRxiv - Genomics 2022Quote: ... each in one lane of an Illumina HiSeq 4000 platform at the UC Davis DNA Technologies Core and according to the manufacturer’s standard protocols (summary statistics of Illumina re-sequencing data per sample is available in Supplementary Table 1).
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bioRxiv - Cancer Biology 2023Quote: ... The first biological replicate of samples was sent to the Health Sciences Sequencing Core at Children’s Hospital of Pittsburgh (HSSC, Pittsburgh, Pennsylvania) for TruSeq ChIP Library preparation (Illumina) using paired indexing ...
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bioRxiv - Developmental Biology 2024Quote: The libraries were sequenced at the NGS (next generation sequencing) Core-Facility of the Leibnitz-Institut für Immuntherapie (LIT) on a NextSeq 550 (Illumina) sequencer ...
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bioRxiv - Molecular Biology 2023Quote: ... The stability of the virus genotype after passage was confirmed via Sanger sequencing and by Illumina sequencing ...
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bioRxiv - Cancer Biology 2019Quote: ... B with the TruSeq RNA Access Library Prep Kit (Illumina). RNA sequencing was performed in HiSeq 2500 (Illumina) ...
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bioRxiv - Microbiology 2023Quote: ... and TruSeq DNA Single Indexes Set A or B (Illumina), excluding the DNA fragmentation and clean-up of fragmented DNA steps ...
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bioRxiv - Cancer Biology 2021Quote: ... ATAC-seq libraries were then sequenced by the University of Manchester Genomic Technologies Core Facility on a HiSeq 4000 System (Illumina).
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bioRxiv - Genetics 2021Quote: ... RNA-seq libraries were constructed by the Genome Technologies core facility at The Jackson Laboratory using the TruSeq RNA Library Prep Kit v2 (Illumina). Libraries were checked for quality and concentration using the DNA 1000 LabChip assay (Agilent Technologies ...
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bioRxiv - Genomics 2020Quote: ... Libraries were prepared by the Genomics unit of the CRG Core Facility (Centre for Genomic Regulation, Barcelona, Spain) with NEBNext ChIPseq Library Prep Reagent Set (ref. E6200S, Illumina) and 50bp sequencing reads were trimmed to remove Illumina adapters and low-quality ends using Trimmomatic (Bolger et al. ...
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bioRxiv - Evolutionary Biology 2021Quote: Sequencing of samples was conducted by the University of Chicago Genomics core using an Illumina HiSeq2500 (Illumina, San Diego, CA) with paired-end 100 base pair reads ...
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bioRxiv - Genomics 2020Quote: ... Single-read sequencing was performed by the Vienna Biocenter Core Facilities (VBCF) for 100 cycles on a HiSeq2500 sequencer (Illumina).
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bioRxiv - Genomics 2020Quote: ... DNA was sent to the UCSF Institute of Human Genetics Core for genotyping using SNP arrays (OmniExpress Exome kit, Illumina).
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bioRxiv - Genomics 2020Quote: ... Paired-end libraries were prepared by the Purdue Genomics Core Facility using the Truseq DNA PCR-Free Sample Preparation Kit (Illumina). Whole-genome sequencing was performed using Illumina short-read technology (2×100bp ...
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bioRxiv - Evolutionary Biology 2019Quote: Sequence reads were first parsed into batches with distinct EcoRI-end adapters based on index sequences at the core facility using CASAVA v1.8 (Illumina, Inc.). We processed reads using the pipeline described in DaCosta and Sorenson (2014 ...
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bioRxiv - Molecular Biology 2020Quote: ... All libraries were sequenced in the sequencing core laboratory at the University of North Dakota on an Illumina MiSeq using protocols and reagents from Illumina. ...
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bioRxiv - Evolutionary Biology 2019Quote: RNA sequencing was carried out at Johns Hopkins School of Medicine Genetic Resources Core Facility on a NovaSeq 6000 sequencing system (Illumina) with a S1 flow cell for 200 cycles ...
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bioRxiv - Microbiology 2019Quote: ... Indexed libraries were pooled and sequenced at the University of Massachusetts Amherst Genomics Core Facility on the NextSeq 550 (Illumina).
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bioRxiv - Genomics 2021Quote: ... Paired-end sequencing was carried out at the Duke Center for Genomic and Computational Biology Sequencing core facility using the Novaseq6000 instrument (Illumina).
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bioRxiv - Microbiology 2020Quote: ... Samples were submitted to Duke Center for Genomic and Computational Biology core sequencing facility for adapter ligation with TruSeq (Illumina) adapters and library amplification ...
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bioRxiv - Systems Biology 2021Quote: ... Sequencing was performed at the Genomics Core Facility (EMBL Heidelberg) with use of the HiSeq2500 platform (Illumina, San Diego, USA) and the run produced 250 bp paired-end reads.
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bioRxiv - Plant Biology 2021Quote: ... were prepared at the Virginia Tech Genomics Core Sequencing Laboratory using the TruSeq Stranded mRNA HT Sample Prep Kit (Illumina), which uses polyA enrichment ...
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bioRxiv - Cancer Biology 2022Quote: ... The samples were sequenced at the Genomic and RNA Profiling Core at Baylor College of Medicine on Nextseq 500 or NovaSeq 6000 sequencing machines from Illumina.
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bioRxiv - Cancer Biology 2022Quote: ... resistant and P12 cells of cell lines #3 and #9 was performed at the Genomics and Proteomics Core Facility of the German Cancer Research Center (GPCF DKFZ, Heidelberg) using the TruSeq DNA PCR-free Methyl protocol (Illumina) for library preparation ...
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bioRxiv - Genomics 2022Quote: ... Library preparation and sequencing was performed by the Innovative Genomics Institute Next-Genration Sequencing Core using MiSeq V2 Micro 2×150bp kit (Illumina). Reads were trimmed and merged (Geneious Prime ...
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bioRxiv - Cancer Biology 2020Quote: Sequencing was performed by the Human & Environmental Genomics core facility of Rennes on a HiSeq 1500 (Rapid SBS kit v2 1×100 cycles, Illumina). Base Calling was performed with Illumina’s CASAVA pipeline (Version 1.8).
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bioRxiv - Cell Biology 2019Quote: ... Libraries were constructed by the Purdue Genomics Core Facilities according to standard protocols using TruSeq Stranded mRNA Library Prep Kit (Illumina). Samples were run on a HiSeq 2500 (Illumina ...
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bioRxiv - Systems Biology 2020Quote: ... DNA was first extracted from stool in line with the Human Microbiome Project’s (HMP) Core Sampling Protocol A (hmpdacc.org) and then sequenced using 2 x 300 bp paired-end sequencing (Illumina MiSeq). Raw sequences were processed using Illumina’s software ...
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bioRxiv - Genomics 2020Quote: ... Libraries were sequenced to 150-bp per read at the Georgia Genomics & Bioinformatics Core (GGBC) on a NextSeq500 platform (Illumina). Average sequencing depth was 41.1x among samples ...
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bioRxiv - Genomics 2020Quote: ... Libraries were sequenced to 150-bp per read at the Georgia Genomics & Bioinformatics Core (GGBC) on a NextSeq500 platform (Illumina). Average sequencing depth was 20.8X among samples (Table S1) ...
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bioRxiv - Physiology 2020Quote: ... High throughput RNA-Sequencing was performed at the NIDDK Genomic Core Facility (NIH, Bethesda, MD) using the HiSeq 2500 instrument (Illumina). Raw sequences were passed through quality control and were mapped to mouse (mm9 ...
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bioRxiv - Genomics 2019Quote: ... Hand > MblRNAi;HA-UPRT and Hand > Bru3;HA-UPRT RNA fractions were mixed at equal concentrations and sequenced (100-bp paired-end reads) on the same lane of a HiSeq 2000 (EMBL Gene Core Illumina Sequencing facility ...
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bioRxiv - Genomics 2019Quote: ... Libraries were sequenced to 150-bp per read at the Georgia Genomics & Bioinformatics Core (GGBC) on a NextSeq500 platform (Illumina). Average sequencing depth was ∼41.1x among samples (Table S7).
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bioRxiv - Immunology 2021Quote: ... Sequencing was performed in the Human Immunology Core Facility at the University of Pennsylvania using an Illumina 2× 300-bp paired-end kit (Illumina MiSeq Reagent Kit v3 ...