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High accuracy DNA sequencing on a small, scalable platform via electrical detection of single base incorporations
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1038/nature03001openalex-snapshot
Finishing the euchromatic sequence of the human genome
inferredcites →https://doi.org/10.1038/nature03959openalex-snapshot
Genome sequencing in microfabricated high-density picolitre reactors
inferredcites →https://doi.org/10.1038/nature07517openalex-snapshot
Accurate whole human genome sequencing using reversible terminator chemistry
inferredcites →https://doi.org/10.1038/nature10242openalex-snapshot
An integrated semiconductor device enabling non-optical genome sequencing
inferredcites →https://doi.org/10.1038/nature24286openalex-snapshot
DNA sequencing at 40: past, present and future
inferredcites →https://doi.org/10.1038/nbt.2835openalex-snapshot
Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls
inferredcites →https://doi.org/10.1038/nbt.4235openalex-snapshot
A universal SNP and small-indel variant caller using deep neural networks
inferredcites →https://doi.org/10.1038/nbt1008-1113openalex-snapshot
How to get genomes at one ten-thousandth the cost
inferredcites →https://doi.org/10.1093/nar/gkn425openalex-snapshot
Substantial biases in ultra-short read data sets from high-throughput DNA sequencing
inferredcites →https://doi.org/10.1101/gr.076463.108openalex-snapshot
A high-resolution, nucleosome position map of C. elegans reveals a lack of universal sequence-dictated positioning
inferredcites →https://doi.org/10.1101/gr.107524.110openalex-snapshot
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
inferredcites →https://doi.org/10.1101/gr.8.3.175openalex-snapshot
Base-Calling of Automated Sequencer Traces Using Phred. I. Accuracy Assessment
inferredcites →https://doi.org/10.1101/gr.8.3.186openalex-snapshot
Base-Calling of Automated Sequencer Traces Using Phred. II. Error Probabilities
inferredcites →https://doi.org/10.1126/science.1162986openalex-snapshot
Real-Time DNA Sequencing from Single Polymerase Molecules
inferredcites →https://doi.org/10.1126/science.1181498openalex-snapshot
Human Genome Sequencing Using Unchained Base Reads on Self-Assembling DNA Nanoarrays
inferredcites →https://doi.org/10.1186/gb-2011-12-11-r112openalex-snapshot
Evaluation of genomic high-throughput sequencing data generated on Illumina HiSeq and Genome Analyzer systems
inferredcites →https://doi.org/10.1186/gb-2013-14-5-r51openalex-snapshot
Characterizing and measuring bias in sequence data
inferredcites →https://doi.org/10.1186/s12859-016-0976-yopenalex-snapshot
Illumina error profiles: resolving fine-scale variation in metagenomic sequencing data
inferredcites →https://doi.org/10.1371/journal.pone.0161333openalex-snapshot
Genome-Wide SNP Calling from Genotyping by Sequencing (GBS) Data: A Comparison of Seven Pipelines and Two Sequencing Technologies
inferredcites →https://doi.org/10.6084/m9.figshare.963153.v1openalex-snapshot
Aligning sequence reads, clone sequences and assembly con*gs with BWA-MEM
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/s10142-021-00810-yopenalex-snapshot
Music of metagenomics—a review of its applications, analysis pipeline, and associated tools
inferred← citeshttps://doi.org/10.1016/b978-0-443-21903-0.00004-7openalex-snapshot
Next-generation sequencing: principles and technical considerations
inferred← citeshttps://doi.org/10.1016/j.yamp.2019.07.012openalex-snapshot
Practical Concepts, Current Challenges, and Technological Advances in Clinical Next-Generation Sequencing Assays for Solid Tumors
inferred← citeshttps://doi.org/10.1155/2024/9943412openalex-snapshot
Circulating Nucleic Acids in Colorectal Cancer: Diagnostic and Prognostic Value
inferred← citeshttps://doi.org/10.1186/s12864-021-08150-8openalex-snapshot
Comparative performance of the GenoLab M and NovaSeq 6000 sequencing platforms for transcriptome and LncRNA analysis
inferred← citeshttps://doi.org/10.1186/s12864-022-08775-3openalex-snapshot
Accuracy benchmark of the GeneMind GenoLab M sequencing platform for WGS and WES analysis
inferred← citeshttps://doi.org/10.6084/m9.figshare.17037636openalex-snapshot
Additional file 1 of Comparative performance of the GenoLab M and NovaSeq 6000 sequencing platforms for transcriptome and LncRNA analysis
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