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Citations for Illumina :
1 - 50 of 133 citations for Guanine Nucleotide Binding Protein G Protein Alpha Activating Activity Polypeptide O GNAO1 Antibody since 2019
Citations are collected from bioRxiv only, the total number of publications could be much larger.
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bioRxiv - Genomics 2019Quote: ... with the flags -m 2 and -g to remove homopolymeric guanine repeats at the end of the reads (a systematic error of Illumina NovaSeq 6000).
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bioRxiv - Microbiology 2022Quote: ... nucleotides in italic represent the Nextera (Illumina) adapter ...
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bioRxiv - Developmental Biology 2024Quote: ... 75-nucleotide sequence reads generated by Illumina sequencing (NextSeq 500 ...
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bioRxiv - Molecular Biology 2023Quote: Trimmomatic version 0.39 was employed to trim reads after a quality drop below a mean of Q20 in a window of 20 nucleotides and keeping only filtered reads longer than 15 nucleotides (Bolger et al., Trimmomatic: a flexible trimmer for Illumina sequence data). Reads were aligned versus Ensembl human genome version hg38 (Ensembl release 104 ...
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bioRxiv - Genomics 2023Quote: ... Trimmomatic version 0.39 was employed to trim reads after a quality drop below a mean of Q15 in a window of 5 nucleotides and keeping only filtered reads longer than 15 nucleotides (Trimmomatic37: a flexible trimmer for Illumina sequence data). Reads were aligned versus Ensembl mouse genome version mm10 (Ensembl release 101 ...
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bioRxiv - Genomics 2021Quote: ... Nucleotide sequences were obtained with a MiSeq instrument (Illumina) in the paired-end 301 bp mode ...
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bioRxiv - Genomics 2020Quote: ... One hundred nucleotides were sequenced using the HiSeq platform (Illumina) from both ends of each cDNA and sequence reads were aligned against the Saccharomyces cerevisiae S288c reference genome using Tophat2 aligner (Kim et al ...
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bioRxiv - Cell Biology 2020Quote: ... Single Nucleotide Polymorphism array Infinium Core-24 v1.1 Kit (Illumina) was used according to manufacturer’s instructions ...
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bioRxiv - Cell Biology 2022Quote: ... One hundred nucleotides were sequenced using the HiSeq platform (Illumina) from both ends of each cDNA ...
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bioRxiv - Genomics 2021Quote: ... Sequencing (single read 50 nucleotides) was performed using a HiSeq2500 (Illumina) with SBS (Sequence By Synthesis ...
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bioRxiv - Molecular Biology 2022Quote: ... The 75-nucleotide paired-end sequencing reads were generated (Illumina, HiSeq 3000) with 6-32 M reads per sample (Supplementary Table 2) ...
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bioRxiv - Cancer Biology 2023Quote: ... Libraries underwent 100 nucleotide paired end sequencing on a NovaSeq 6000 (Illumina).
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bioRxiv - Plant Biology 2023Quote: An Illumina Infinium SNP (Single Nucleotide Polymorphism) array (Illumina, Inc., San Diego, USA) developed by Plomion et al ...
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bioRxiv - Plant Biology 2023Quote: ... mRNA stranded nucleotide libraries were created by fusing TruSeq RNA sequencing adapters (Illumina), followed by library amplification by PCR ...
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bioRxiv - Microbiology 2023Quote: ... with 6 nucleotides library indexes (DNA Single Indexes Set A or B, Illumina). To achieve sufficient variability during the first five sequencing cycles ...
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bioRxiv - Genomics 2023Quote: ... The nucleotide sequences of the resultant libraries were determined using HiSeq 1000 (Illumina) in paired-end ...
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bioRxiv - Genomics 2023Quote: ... cycle one begins with incorporation of the first nucleotide in Incorporation Mix (Illumina MiSeq), followed by incubation with shaking at 60°C for 3 min ...
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bioRxiv - Cancer Biology 2023Quote: ... Libraries were sequenced using 100 nucleotide paired-end sequencing on a NovaSeq 6000 (Illumina).
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bioRxiv - Plant Biology 2023Quote: The prediction of protein-coding potential for transcripts generated from Illumina and SMRT data was conducted by integrating CPC2 v0.1 ...
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bioRxiv - Molecular Biology 2019Quote: ... The fluorescent images were processed to nucleotide sequences using the analysis Pipeline supplied by Illumina.
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bioRxiv - Genomics 2019Quote: ... DNA was genotyped at 719,665 single nucleotide polymorphisms (SNPs) using the HumanOmniExpress-24 BeadChip (Illumina). The SNP call rate was > 97% in all donors ...
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bioRxiv - Cancer Biology 2020Quote: ... Sequencing of 75 nucleotide-long paired-end reads was performed in a NextSeq-500 (Illumina).
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bioRxiv - Cancer Biology 2020Quote: ... Sequencing of 75 nucleotide-long single-end reads was performed in a NextSeq-500 (Illumina).
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bioRxiv - Biochemistry 2021Quote: ... Libraries were sequenced using paired end sequencing length of 75 nucleotides on a HiSeq4000 machine (Illumina).
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bioRxiv - Cancer Biology 2020Quote: Single nucleotide polymorphism (SNP) arrays were performed on the Global Screening Array-24 v2-0 (Illumina) and scanned on an iScan (Illumina ...
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bioRxiv - Cell Biology 2023Quote: ... RNA-seq libraries were subjected to paired-end sequencing (53 nucleotides each) on NovaSeq 6000 (Illumina) using a NovaSeq 6000 SP Reagent Kit (Illumina) ...
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bioRxiv - Molecular Biology 2023Quote: ... and cell surface protein libraries were sequenced on the NextSeq 550 System (Illumina).
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bioRxiv - Microbiology 2021Quote: ... Single-end reads of 65 nucleotides (nt) in length were generated on a HiSeq2500 sequencing platform (Illumina). Reads were cleaned of adapter sequences ...
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bioRxiv - Genomics 2022Quote: ... The genome integrity was assessed by a single nucleotide polymorphism-based karyotyping assay (Illumina, HumanOmniExpress-24 v1.1). The iPSCs were maintained in a defined E8 medium (Life Technologies ...
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bioRxiv - Cell Biology 2019Quote: ... Libraries were sequenced using paired eind sequencing length of a 100 nucleotides on a HiSeq4000 machine (Illumina).
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bioRxiv - Genomics 2021Quote: ... Nucleotide sequences of the libraries were determined with theHiSeq 2500 DNA sequencing system (Illumina, San Diego, CA) in paired-end ...
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bioRxiv - Molecular Biology 2023Quote: CAGE libraries were sequenced using single end reads of 75 nucleotides on a NextSeq 500 instrument (Illumina). The obtained reads (CAGE tags ...
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bioRxiv - Microbiology 2023Quote: ... An Illumina NextSeq sequencer was applied for generation of paired-end fragment reads (2 × 150 nucleotides) and bcl2fastq software (v2.17.1.14; Illumina) was applied for primary data analysis (base-calling) ...
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bioRxiv - Genomics 2024Quote: ... Paired end (2 × 250 nucleotides) sequencing of the library was performed in a Novaseq 6000 (Illumina Inc.) next-generation DNA sequencer ...
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bioRxiv - Genomics 2024Quote: ... Twenty individual resequencing datasets were downloaded from the European Nucleotide Archive (ENA: 150-bp paired-end, Illumina sequencing data ...
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bioRxiv - Genetics 2021Quote: ... The detection of the nucleotide sequence was done on the Illumina NovaSeq6000 platform using the according kit (Illumina).
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bioRxiv - Genetics 2019Quote: Micro-array analysis was performed using the single-nucleotide polymorphism (SNP) CytoSNP-850Kv0 BeadChip (Illumina Inc., San Diego) using standard protocols and the GenomeStudio genotyping module (v1.9.4 ...
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bioRxiv - Microbiology 2020Quote: ... Isolated RNA was heat fragmented and libraries were prepared for 2 × 250 nucleotide paired-end sequencing performed (Illumina). Genewiz performed basecalling and read demultiplexing.
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bioRxiv - Genetics 2022Quote: ... ROH were initially mapped by genome-wide single-nucleotide polymorphism (SNP) chip analysis (HumanCytoSNP-12 BeadChip platform, Illumina). ROH (>1 Mb ...
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bioRxiv - Molecular Biology 2020Quote: ... NCBI build 37) was carried out using the Efficient Local Alignment of Nucleotide Data algorithm (Eland, Illumina, Inc) as described previously (Yuan et al ...
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bioRxiv - Molecular Biology 2022Quote: ... generated by Illumina HiSeq 2000 platform were converted into nucleotide sequence with quality score FASTQ (FASTA with quality score) using CASAVA software v1.8.2 (Illumina) followed by adaptor trimming ...
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bioRxiv - Developmental Biology 2021Quote: ... On average 10.6 millions of 38-nucleotide paired-end sequences were obtained using a NextSeq 500 sequencer (Illumina).
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bioRxiv - Genomics 2022Quote: In order to map SNP markers from the 65K single nucleotide polymorphism (SNP) array (65,000 SNP; Illumina, Inc.) to the new genome build we first aligned the two genome builds (Turkey_5.1 and Mgal_WU_HG_1.0 ...
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bioRxiv - Neuroscience 2022Quote: ... B allele frequency and log R ratio of each single nucleotide polymorphism (SNP) marker were collected from GenomeStudio (Illumina) and analyzed with PennCNV [70] and QuantiSNP [10] with default parameter settings ...
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bioRxiv - Microbiology 2024Quote: ... One hundred nucleotides of sequence were determined from both ends of each cDNA fragment using the Novaseq platform (Illumina). Sequencing reads were aligned to the reference genomes (C ...
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bioRxiv - Molecular Biology 2021Quote: ... and nucleotide sequences were generated using a NextSeq 500 and a NextSeq 500/550 High Output v2 kit (75 cycles) (Illumina).
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bioRxiv - Molecular Biology 2019Quote: Poly (A)-containing mRNA from each sample was used to prepare libraries using NEXTflex qRNA-seq Kit for 125 nucleotide single-end sequencing by Illumina HiSeq 2500 ...
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bioRxiv - Microbiology 2020Quote: ... Paired-end sequencing of 300-nucleotide fragments was performed using the MiSeq reagent kit V3 on a MiSeq System (Illumina). Taxonomic analysis was performed with QIIME2 (59) ...
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bioRxiv - Microbiology 2020Quote: 150 nucleotides of the sequence were determined from both ends of each cDNA fragment using the HiSeq 2500 platform (Illumina). An average of 83.79 million read pairs were obtained for each sample (range ...
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bioRxiv - Microbiology 2020Quote: ... Seventy-five nucleotides of the sequence were determined from both ends of each cDNA fragment using the HiSeq 4000 platform (Illumina). Sequencing reads were aligned to the reference R ...