The DOI matches its Crossref record; 22 of the 24 references it cites were found in a registry or an index.
Fast and accurate long-read alignment with Burrows-Wheeler transform.
Open accessAbstract
Motivation: Many programs for aligning short sequencing reads to a reference genome have been developed in the last 2 years. Most of them are very efficient for short reads but inefficient or not applicable for reads >200 bp because the algorithms are heavily and specifically tuned for short queries with low sequencing error rate. However, some sequencing platforms already produce longer reads and others are expected to become available soon. For longer reads, hashing-based software such as BLAT and SSAHA2 remain the only choices. Nonetheless, these methods are substantially slower than short-read aligners in terms of aligned bases per unit time. Results: We designed and implemented a new algorithm, Burrows-Wheeler Aligner's Smith-Waterman Alignment (BWA-SW), to align long sequences up to 1 Mb against a large sequence database (e.g. the human genome) with a few gigabytes of memory. The algorithm is as accurate as SSAHA2, more accurate than BLAT, and is several to tens of times faster than both. Availability: http://bio-bwa.sourceforge.net Contact: rd@sanger.ac.uk
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“Software confirmed to be working for this approach include (but are not limited to) Bowtie2 11, BWA 12, HISAT2 13, STAR 14 or any tool wrapping one of these aligners.”
From SNPsplit: Allele-specific splitting of alignments between genomes with known SNP genotypes (2016) · cites this paper as [12]
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“Mapping reads to specific genes is relatively straightforward with the bioinformatics tools available today [10-13], but using these tools to distinguish between reads derived from alternative alleles of the same gene remains challenging [9].”
From Sources of bias in measures of allele-specific expression derived from RNA-seq data aligned to a single reference genome (2013) · cites this paper as [11]
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Gapped BLAST and PSI-BLAST: a new generation of protein database search programs
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The Sequence Alignment/Map format and SAMtools
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Self-citationFast and accurate short read alignment with Burrows-Wheeler transform
Li, H., & Durbin, R. (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp324 · Cited by 58,607
Self-citationUltrafast and memory-efficient alignment of short DNA sequences to the human genome.
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Influential<tt>BLAT</tt> —The <tt>BLAST</tt> -Like Alignment Tool
Kent, W. J. (2002) · Genome Research · doi:10.1101/gr.229202 · Cited by 8,480 · cited 1×
“…and PatternHunter (Ma et al ., 2002), greatly speeding up matching capillary sequencing technologies arrived that generated millions of short (<100bp) reads, a variety of new algorithms were developed which were 10–1000 times faster, including SOAP (Li,R. et al 2008), MAQ (Li,H. et al ., 2009).”
A Greedy Algorithm for Aligning DNA Sequences
Zhang, Z., Schwartz, S., Wagner, L., & Miller, W. (2000) · Journal of Computational Biology · doi:10.1089/10665270050081478 · Cited by 5,459 · cited 1×
“…SSAHA2 (Ning et al ., 2001), BLAT (Kent, 2002) and PatternHunter (Ma et al ., 2002), greatly speeding up matching capillary sequencing technologies arrived that generated millions of short (<100bp) reads, a variety of new algorithms were developed which were 10–1000 times faster, including…”
SOAP: Short oligonucleotide alignment program
Li, R., Li, Y., Kristiansen, K., & Wang, J. (2008) · Bioinformatics · doi:10.1093/bioinformatics/btn025 · Cited by 3,597
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Li, H., Ruan, J., & Durbin, R. (2008) · Genome Research · doi:10.1101/gr.078212.108 · Cited by 2,638 · cited 1×
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Self-citationReal-time DNA sequencing from single polymerase molecules.
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- Burrows, 1994, A block-sorting lossless data compression algorithm
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Items 1,001–1,100 of 1,225
Unique sex chromosome translocations and evolutionary strata in two Sylvioidea songbird families
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“FindZX is openly available at GitHub ( h t t p s : / / g i t h u b . c o m / h s i g e m a n / fi n d Z X) and implements commonly used software, including BWA-MEM [41, 42] for read alignment, SAMtools [43] for filtering aligned read, and Platypus [44] for variant calling.”
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“1) using bwa mem 62 .”
Zheng, Y., Qi, F.-Y., Shi, L., Sun, Z.-Q., Liu, H.-F., Liu, H., Qin, L., Wang, J., Zhi, C.-Y., Wang, M.-M., et al. (2026) · Plant Biotechnology Journal · doi:10.1111/pbi.70667
“Clean reads were mapped to the reference genome using BWA (version 0.7.17-r1188) (Li and Durbin 2010).”
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Amr, K. S., Ahmed, H. A., Shalabi, T., Abdel-Hady, S., & El-Bassyouni, H. T. (2026) · Molecular Biology Reports · doi:10.1007/s11033-026-11701-5
Wang, K., Li, J.-H., Liu, T.-Y., Li, P., Wang, N., Liu, Y., Liang, Y., Li, F., Wei, C., Yan, H., et al. (2026) · Emerging Microbes and Infections · doi:10.1080/22221751.2026.2660424
“1), was used for read mapping with BWA version 0.7.18 and SAMtools version 1.20.0 [15, 16].”
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“48) using BWA [21], and interacting segment pairs were computed with Pairtools [22].”
Zhang, H., Mao, W., Lai, Z., Zhu, Y., Dong, J., Li, L., Xie, F., Zhu, W., Shen, J., & Mao, S. (2026) · Microbiome · doi:10.1186/s40168-026-02397-7 · Cited by 1
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“7.17) [24].”
InfluentialTronsgaard, S., Quintela, M., Vihtakari, M., Dahle, G., Besnier, F., Bradbury, I. R., Hansen, M. M., Glover, K., & Jorde, P. (2026) · BMC Research Notes · doi:10.1186/s13104-026-07806-6
“In 2019, reads of pool genome sequencing of female and male Atlantic halibut were mapped independently to a draft reference genome available at the time (Rolf Edvardsen, personal communication)— and later on published as Edvardsen et al., [10]— using the BWA aln function [31].”
Zhe, M.-Q., Zhang, Z.-X., & Sun, Y.-B. (2026) · Integrative Zoology · doi:10.1111/1749-4877.70112
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“Reads were mapped using BWA-SW, version 0.7.15-r1140, settings bwasw-b7 (Li and Durbin, 2010).”
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“1 [15, 16].”
INAEME: Integral Neoantigen Analysis with Entirety of Mutational EventsPreprint
Kovačević, V., Milicevic, O. S., Raicevic, N. I., Kojicic, M., Lazic, A. M., Skundric, N., & DiGiovanna, J. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.09.28.559901
“The first step performs read alignment [23], leveraging GATK best practices.”
Hou, X.-B., Chen, B.-L., Zou, Z.-Y., Zhu, J.-L., Li, D.-Y., Yu, J., Yang, H., & Xiao, W. (2026) · Conservation Genetics Resources · doi:10.1007/s12686-026-01427-8
“7.17 (Li and Durbin 2010 ).”
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“Quality and contamination filtered individual reads were mapped onto the reference catalogue using the Burrows-Wheeler Aligner v 0.7.13 (Li and Durbin 2010).”
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“7.17 [16] with the mem algorithm.”
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“7.17 [30].”
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Nissan, Y., Inbar, S., Privman, E., Yovel, Y., & Razgour, O. (2026) · Evolutionary Applications · doi:10.1111/eva.70243
“7.17 (Li and Durbin 2010), was used to aligned the reads to the reference genome ‘mRouAeg1.p’ assembly (Jebb et al. 2020) and SAMTOOLS v1.”
InfluentialGe, D., Gao, G., Dargye, L., Zou, R., Jin, J., Ning, C., Liang, G., & Zhang, Q. (2026) · Journal of Archaeological Science Reports · doi:10.1016/j.jasrep.2026.105616
Zhou, Y.-X., Wu, W.-G., Luo, W.-K., Chang, L., Mo, M., Leng, L., Gao, B., Zeng, J., He, W., Ning, J., et al. (2026) · The Plant Journal · doi:10.1111/tpj.70858
Lu, S.-S., Xia, Y., Sun, Q.-Y., Sun, Y.-H., Chen, R., Jin, H., Zhang, J., Liu, W., & Huang, J. (2026) · Journal of Inflammation Research · doi:10.2147/jir.s581751
First multi-individual Neanderthal mitogenomes from north of the Carpathians
Picin, A., Hajdinjak, M., Nowaczewska, W., Blaauw, M., Bayliss, A., Fewlass, H., Heaton, T., Reimer, P. J., Southon, J. R., van der Plicht, J., et al. (2026) · Current Biology · doi:10.1016/j.cub.2026.03.069
Yuan, Y., Wang, J.-H., Zhang, P., Guo, Y., Wang, Z., Liu, S., & Jia, Z.-R. (2026) · Flora: Morphologie, Geobotanik, Oekophysiologie · doi:10.1016/j.flora.2026.152987
A Novel Phosphoglucomutase-3 Gene Variant Causing Milder Phenotype in Two Families
Karaaslan, B. G., Benamar, M., Ulaş, S., Aydemir, S., Yeşil, G., Gezdirici, A., Sarı, A. A., Nepesov, S., Çokuğraş, H., Camcıoğlu, Y., et al. (2026) · Journal of Clinical Immunology · doi:10.1007/s10875-026-02012-2
The diversity of insecticide target site mutations in Apis mellifera
Verbinnen, G., Smet, L. D., Henriques, D., Tytgat, J., Pinto, M. A., & de Graaf, D. D. (2026) · BMC Genomics · doi:10.1186/s12864-026-12770-3
“1) using the Burrows-Wheeler Aligner 0.7.17 [112].”
InfluentialLv, C., Chen, L.-L., Zou, P., Chen, Y., & Ma, Y. (2026) · BMC Genomics · doi:10.1186/s12864-026-12722-x
“7.17 (BWA) algorithm [10].”
InfluentialThe pQBR mercury resistance plasmids: a model set of sympatric environmental mobile genetic elements
Orr, V. T., Harrison, E., Rivett, D., Wright, R. C. T., & Hall, J. (2026) · bioRxiv · doi:10.1099/mgen.0.001789
“To identify plasmid sequences, reads were first mapped against reference Pseudomonas chromosomes using ‘bwa-mem’ [46], and reads that did not map to the chromosome were extracted using SAMtools [47].”
Jiang, Y.-Z., Pu, Y.-F., Huang, Z., Pei, Q., Li, M., & Xu, M.-F. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1727070
Byers, A.-K., Condron, L., Wairapa, N., & Black, A. (2026) · Ecology and Evolution · doi:10.1002/ece3.73274
DNA Virus Detection in Olfactory Neuroblastomas Using Targeted Enrichment NGS
Jauhiainen, M., Mielonen, O., Haapaniemi, A., Söderlund-Venermo, M., Hagström, J., Perdomo, M. F., Sinkkonen, S., & Mäkitie, A. (2026) · Neuropathology (Kyoto. 1993) · doi:10.1111/neup.70055
“For aligning the reads, we used the Burrows–Wheeler alignment tool [31] and reconstructed the consensus sequences (SAMtools, BCFtools) [32].”
Lan, L., Zhang, X., Xie, J., Lin, X., Hong, X., Nie, W.-H., Wang, J.-H., Su, W., Yang, F., He, G.-M., et al. (2026) · Molecular Ecology Resources · doi:10.1111/1755-0998.70129
“Second, we estimated the mapping rate through minimap2 v 2.24-r1122 (Li 2018) for Nanopore long reads and bwa v 0.7.17-r1188 (Li and Durbin 2010) for Illumina short reads and RNA-seq reads.”
InfluentialPan, B.-Z., Zhang, X., Hu, X.-D., Fu, Q.-T., Chen, M.-S., Tao, Y.-B., Niu, L.-J., He, H.-Y., Shen, Y., Cheng, Z.-K., et al. (2026) · bioRxiv · doi:10.64898/2026.03.18.712556
“To evaluate the assembly quality, Illumina reads (27.24 Gb of data, ~35.26 X) from the 220 bp library were mapped to the assembled genome with BWA (Li and Durbin, 2010).”
InfluentialInsights into spacer acquisition of the type V-A CRISPR–Cas system of Francisella novicida U112
Hille, F., Wang, C., Finstermeier, K., Beerens, D. M. J. M., Schmidt, K., Skibbe, M., & Charpentier, E. (2026) · Nucleic Acids Research · doi:10.1093/nar/gkag276
“T 22 to accommodate the short nature of the spacers [ 60 ] as well as Samtools V 1.20-17-g078b220 [ 61 ].”
InfluentialHitchcock, N. B., Annoh, M., Grassi, L., Das, S., Ferreira, C. S., Ray, D., Elgendy, R., Wang, L., Lee, K., Sudbery, I. M., et al. (2026) · bioRxiv · doi:10.64898/2026.03.16.712126
Rapid Genomic Adaptation of Drosophila Melanogaster to Wolbachia Elimination
Dou, W., & Li, T.-C. (2026) · Microbial Ecology · doi:10.1007/s00248-026-02732-3
“7.17 [ 36 ].”
InfluentialHan, X.-X., Yin, J., Jiao, X., Hu, R., Zhang, Y., Chen, F., Dong, B., Cheng, C., Wang, Y.-H., Wang, C.-H., et al. (2026) · TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · doi:10.1007/s00122-026-05195-9
Hao, X., Hu, X., Pan, Y., Zhang, Q., Ou, R., Jiang, F.-F., Liu, F., Zhang, J.-P., Wang, W., Xing, G.-N., et al. (2026) · Journal of Integrative Plant Biology · doi:10.1111/jipb.70223
“Reads were aligned to the reference genome Williams 82 (Wm82.a2.v1) via BWA ‐ mem (Li and Durbin, 2010), and SNPs were called using GATK HaplotypeCaller and SAMtools mpileup (DePristo et al., 2011; Danecek et al., 2021).”
Liang, Y.-X., Liu, T.-T., Zhang, C.-P., Gao, J., Dai, M., Xu, Z.-F., Qiao, F.-C., & Wang, Y. (2026) · Journal of Maternal-Fetal & Neonatal Medicine · doi:10.1080/14767058.2026.2640649
Xiao, Y., Chen, L., Han, Y.-C., Luo, J.-F., Wang, M.-M., Ai, Y., Liu, W., Xiong, W.-P., Jin, Y., Kong, S., et al. (2026) · EBioMedicine · doi:10.1016/j.ebiom.2026.106211
Population genomics of Quercus gilva provides insights into the conservation of fengshui forests
Jiang, X.-L., Wu, M.-X., Saito, Y., Luo, S.-S., Liu, X.-S., Ouyang, Z.-Y., Li, J.-X., Deng, M., & He, L. (2026) · Communications Biology · doi:10.1038/s42003-026-09846-x
Lu, N., Wang, T., & Li, Y. (2026) · International Conference on Bioinformatics and Intelligent Computing · doi:10.1145/3809986.3809997
“Preprocessed reads were aligned to hg19 using BWA-MEM [18].”
Laforest, M. F., Bessette, M., Gagnon, G., Flores‐Mejia, S., Soufiane, B., Goulet, M., & Michaud, D. (2026) · Pest Management Science · doi:10.1002/ps.70721
Aleshina, O. A., Vasileva, A. N., Сергеевна, К. Е., Вениаминовна, Б. Б., & Parovichnikova, E. N. (2026) · Oncohematology · doi:10.17650/1818-8346-2026-21-1-22-32
Metagenomic sequencing of zoonotic viruses: evaluation of a CRISPR-Cas-based rRNA depletion system.
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“7.12 (Li and Durbin, 2010) and standard parameters.”
InfluentialRen, L., Han, X., Wang, Q.-X., Yang, K., Zhang, J., Zhang, R.-Y., Wang, Y.-D., Zeng, Y., Liu, L., Liu, W., et al. (2026) · Comparative Biochemistry and Physiology - Part D:Genomics and Proteomics · doi:10.1016/j.cbd.2026.101798
Zeng, Y., Zhang, J., Wang, Q.-X., Han, X., Liu, L., Yang, K., Zhang, R.-Y., Luo, K.-K., Ren, L., & Liu, S. (2026) · Comparative Biochemistry and Physiology - Part D:Genomics and Proteomics · doi:10.1016/j.cbd.2026.101787
Sun, X., Wang, C., Lin, L., Lan, X., Wu, S., Chen, X., & Cai, C. (2026) · Scientific Reports · doi:10.1038/s41598-026-40703-3
“7.15) 12 .”
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“2.1) [66,67], and two successive rounds of polishing were performed using Pilon (v1.”
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Modestov, A., Luppov, D. V., Gaziev, I., Golushko, N., Захарова, Г. С., Zolotovskaia, M., Poddubskaya, E. V., Seryakov, A. P., Prassolov, V., Игоревна, С. М., et al. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27062625
“7.17 [85].”
InfluentialThe Inheritance Puzzle: A Case of Dual Genetic Kidney Disease
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“M), iterating until Merqury QV and BUSCO scores plateaued [48,49].”
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“M and - t 8’ was used to align reads for each strain to the assembly of one reference strain in each clade (Clade A: BF1, Clade B: SB1, Clade C: W2, Clade D: ALR11; Li and Durbin 2009, 2010).”
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Interspecies hybridization as a route of accessory chromosome origin in fungal pathogens
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Wang, M.-X., Hu, G.-J., Yangjin, L., Zeng, S., Xiong, H.-Y., He, T., & Duan, R.-Q. (2026) · Scientific Data · doi:10.1038/s41597-026-06931-y
Barbosa, D. A., de Maria, Y. N. L. F., Menegídio, F. B., de Oliveira, R. C., Jabes, D. L., & Nunes, L. R. (2026) · Archives of Virology · doi:10.1007/s00705-026-06522-7
“Reads were mapped to the Mus musculus mm10 genome using BWA-MEM [29], and host sequences were removed using Samtools view and SamToFastq [ 30 ].”
Jiang, X., Chen, C., Zhao, M., Hu, L., Shi, L., Tang, T., Lv, B., Ji, S., Jia, L., Pang, J., et al. (2026) · BMC Genomics · doi:10.1186/s12864-026-12645-7
“7.17 [42], and the resulting alignments were stored in BAM format.”
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“This efficiency has made the FM index a workhorse in genomics [18, 20], yet even space close to the plain-text representation can be prohibitive at massive scales.”
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Ruiz-Corzo, B., Casado-García, A., Oak, N., Somoza-Cotillas, P., de Neyra, A. L.-Á., Martínez-Cano, J., Pérez‐Pons, A., Sánchez, E. G., Blanco, Ó., Alonso‐López, D., et al. (2026) · JCI Insight · doi:10.1172/jci.insight.199464
“Illumina paired-end reads were preprocessed and were mapped to the mouse reference genome (mm10) with BWA (33).”
Maleknia, S., Hassoun, R., Adra, N., & Shahbazi, R. (2026) · Molecular Biomedicine · doi:10.1186/s43556-026-00405-8
“In Partek ® Flow ® software, this task was executed via aligning reads to the hg38 reference genome using Burrows-Wheeler Alignment (BWA) [31] approach.”
Chromosome-level genome assembly of the sponge Halisarca dujardinii
Zubarev, V. M., Cherkasov, A., Sidorov, L., Adameyko, K. I., Finoshin, A. D., Ryabova, A., Kashtanova, A., Gazizova, G. R., Gogoleva, N. M., Burakov, A. V., et al. (2026) · Scientific Data · doi:10.1038/s41597-026-07161-y
Yousaf, H., Ali, S., Moulvi, A., Khalid, L. B., Javed, I., Ghumman, R., Colson, C., Ibrahim, S., Zia, S., Khan, M., et al. (2026) · Human Genomics · doi:10.1186/s40246-026-00914-1
“Raw reads were aligned to hg38 using BWA MEM 0.7.17 [34].”
InfluentialA chromosome-level reference genome for Pacific herring (Clupea pallasii) from the Bering Sea
Timm, L. E., Hsieh, Y.-C., López, J. A., Almgren, S. A., & Glass, J. (2026) · bioRxiv · doi:10.46471/gigabyte.182
“7.17 [16], skipping pairing (–”
InfluentialChromosome-level genome assembly of mud snail Bullacta exarata
Xie, X., Wang, S., Sun, Y., Bai, Y.-A., Li, H.-L., Li, D.-C., Liu, X.-F., Teng, W., Li, X., & Wang, Q. (2026) · Scientific Data · doi:10.1038/s41597-026-06791-6
“7.17) 14 .”
InfluentialSelf-citationWünschmann, T., Ghaderiardakani, F., Homeier-Bachmann, T., Quartino, M., Wichard, T., & Busch, A. (2026) · BMC Genomics · doi:10.1186/s12864-026-12626-w
“Illumina reads were mapped to the polished consensus sequence using BWA-MEM2 (Galaxy version 2.2.1 + galaxy1) [32].”
InfluentialReference genome choice impacts SNP recovery but not evolutionary inference in young speciesPreprint
Soares, L. S., Gonçalves, L. T., Guzmán-Rodriguez, S., Bombarely, A., & Freitas, L. B. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.04.703758 · Cited by 1
“7.10-r789 (Li & Durbin, 2010).”
InfluentialGenome survey of nutmeg (Myristica fragrans) from Indonesia: genomic resource for Myristicaceae
Cartealy, I., Wulandari, D. R., Tajuddin, T., Salamah, A., Bismantoko, S., Nugraha, I., Bissa, S. Y. C., & Abinawanto, A. (2026) · Frontiers in Plant Science · doi:10.3389/fpls.2026.1753954
“7.17 (Li and Durbin, 2010), and taxonomy information of the contigs by searching the contigs against the NCBI non-redundant (nt) database using MMseqs2 v17-b804f (Steinegger and Söding, 2017), respectively.”
InfluentialMkpuma, N., Meseko, C., Shittu, I., Chukwu, C., Afiukwa, F. N., Iroha, I., Muhammad, M., & Ogbu, O. (2026) · BMC Veterinary Research · doi:10.1186/s12917-025-05279-6
“7.12 [40].”
InfluentialMin, D., Jang, Y.-J., Kim, Y., & Lee, G. (2026) · Horticultural Science and Technology · doi:10.7235/hort.20260002
Key Genomic Regions of Rice Cultivar GuiHeFeng and Its Derivatives Revealed by Genome-Wide Analysis
Chen, Y.-Z., Hao, X., Zhang, Y.-X., Ma, Z., Liu, C., Zhou, X., Wei, M., Qin, B.-X., Yan, Y., & Huang, D.-H. (2026) · Plants · doi:10.3390/plants15030520
“7.12) [58].”
InfluentialZhang, Y., Yuan, P., Wang, B.-Z., Gao, L.-N., Wang, B.-N., Hao, X.-P., Guo, L., & Ying, J.-M. (2026) · Translational Lung Cancer Research · doi:10.21037/tlcr-2025-1130
“7.12) (23).”
InfluentialHe, J., Wang, L., Yu, L., Wu, X., Yan, Z., Ning, C., Zhang, F., & Song, G. (2025) · Journal of Archaeological Science · doi:10.1016/j.jas.2025.106452
Ge, D., Duan, C., Zhang, Z., Zhang, H., Zhang, J., Jin, J., Zou, R., Zhang, Q., Jing, X., He, J., et al. (2026) · Journal of Archaeological Science · doi:10.1016/j.jas.2026.106479
Kiedaisch, T., Gautier, L., Boluda, C., Pouchon, C., & Naciri, Y. (2026) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2026.108569
Okunola, A., Loubser, J., Ghielmetti, G., Gumbo, R., Streicher, E. M., Ncube, P., Dippenaar, A., Goosen, W., Guimarães, A. M. S., Warren, R., et al. (2026) · Microbial Genomics · doi:10.1099/mgen.0.001646
“15 [41, 42].”
Rare Germline Variants in CDKN2A ‐Negative Children and Adolescents With Cutaneous Melanoma
Johansson, P. A., Palmer, J. M., Bui, L. T., Xu, M., Jones, K. M., Higson, H., Liu, J., Brooks, K. M., Pritchard, A. L., Hayward, N. K., et al. (2026) · Pigment Cell & Melanoma Research · doi:10.1111/pcmr.70079 · Cited by 1
“Sequence reads were mapped to the HumanG1Kv37 assembly using BWA (Li and Durbin 2010), sorted with samtools (Li et al. 2009), and duplicate reads were marked with Picard.”
Morgenstern, D., Hamilton, B., Korbie, D., Clauser, K. R., Haas, B., Bowlay, G., Voje, K., Jones, A., Venter, D. J., King, G., et al. (2026) · Toxicon · doi:10.1016/j.toxicon.2026.109026
Pan, L., Wang, J., Tang, P., Li, Y.-L., Luo, Y., Miao, W., Huang, J., Wang, M., Xie, L., Hu, C.-X., et al. (2026) · Journal of Integrative Agriculture · doi:10.1016/j.jia.2026.02.031
Li, C., Erson-Omay, E., Koksal, Y., Unal, E., Kara, B., Bilguvar, K., Paksoy, Y., Durmuş, N., Kurtsoy, A., Per, H., et al. (2026) · iScience · doi:10.1016/j.isci.2026.115029
Ahmad, S., Khan, B., Shams, H., Sao, G. H., Gul, A., Khang, R., Khan, S., & Kalsoom, U. (2026) · Clinical Dysmorphology · doi:10.1097/mcd.0000000000000552
Lol, J. C., Böhmert, A. L., Hartke, J., Sanou, A., Kerbl-Knapp, J., Morris, M., Mäurer, J. B., Hogan, P., Guelbeogo, M. W., Lucas, E. R., et al. (2026) · BMC Genomics · doi:10.1186/s12864-026-13109-8 · Cited by 1
Kohanbash, G., Ryall, S., Gary, S., Hoffman, L., Siddaway, R., Bendel, A., Gripp, K., Walter, A. W., Hansford, J., Smith, A. A., et al. (2026) · Research Square · doi:10.21203/rs.3.rs-8662616/v1
“7.8 [25], and processed with the GATK suite [26].”
InfluentialMPXV RNA-seq data provide evidence for protection of viral transcripts from APOBEC3 editing
Lyskova, A. O., Abasov, R. K., Pavlova, A. V., Matveev, E., Madorskaya, A. V., Kazanov, F. M., Garshina, D. V., Smolnikova, A. E., Ponomarev, G. V., Sharova, E., et al. (2026) · Journal of Virology · doi:10.1128/jvi.02082-25
“Short-read RNA-seq data were aligned using STAR (version 2.7.11b) (32), and genomic DNA short reads were mapped using BWA (version 2.2.1) (33).”
InfluentialYap, Z. L., Yi, S., Quintana, E., García, L., Safklou, M., Darragh, R., Hogan, A. M., Motnenko, A., Blunt, W., Sparling, R., et al. (2026) · bioRxiv · doi:10.1128/aem.00142-26
Liu, C., Tu, C., Li, P., Wu, H., Wan, F., Lu, Y., Tang, S., Li, X., Li, K., Wang, J., et al. (2026) · Science China Life Sciences · doi:10.1007/s11427-025-3186-2
Goonetilleke, S. N., Wilkinson, M. J., Wirthensohn, M., Collins, C., Furtado, A., Henry, R., & Hardner, C. M. (2026) · bioRxiv · doi:10.64898/2026.01.22.701136
“7.15-r1140 (Li and Durbin 2010).”
InfluentialWang, S., Liu, C., Yang, M., Yang, D., Pang, H., Wang, F., Yè, G., Fang, Q., Ye, X., & Yang, Y. (2026) · Biology · doi:10.3390/biology15030214
“Sequence consistency analysis showed alignment rates of 98.53% and 98.79% to the assembly [21–24].”
InfluentialWen, S., Cheng, C., Yin, J.-Y., Lv, Y., Zhang, X., Ma, B., Liu, Y., Qiu, Y.-S., He, H., Luo, P., et al. (2026) · Biology · doi:10.3390/biology15030208
“7.19 [22].”
InfluentialProctor, R., Busman, M., Kim, H.-S., Menke, J., Villani, A., Lohmar, J., Brown, D. W., Turgeon, B., Susca, A., Moretti, A., et al. (2026) · BMC Genomics · doi:10.1186/s12864-025-12037-3
“Reads were aligned to the draft PacBio assembly following the manufacturer’s recommendations using BWA-MEM with the − 5SP and -t 8 options specified, and all other options default [41].”
iSCoder: Mitigating Genomic Sequencing Data Compression Bottlenecks via In-SRAM Computing
Liu, W., Li, Y.-W., & Tan, G. (2026) · Journal of Computational Science and Technology · doi:10.1007/s11390-025-5022-y
A new integrated genetic and transcriptomic approach for investigating DUX4 and DUX4C
Zhuang, Z., Ueda, M., Yamaguchi, K., & Kochi, Y. (2026) · Journal of Human Genetics · doi:10.1038/s10038-025-01450-x
“7.19 with default parameters [13].”
InfluentialCampbell, M. A., Hale, M., Balachandran, N., Chen, W.-J., & Becker, J. A. (2026) · Conservation Genetics · doi:10.1007/s10592-025-01751-w
“2 with the Burrows-Wheeler aligner with the mem algorithm (bwa mem) (Li and Durbin 2009, 2010).”
Caruso, L. B., Maestri, D., Kossenkov, A., Goldman, A. R., Cassel, J., Soldan, S. S., Lieberman, P., & Tempera, I. (2026) · bioRxiv · doi:10.64898/2026.01.12.699161
A compendium of chromatin interaction maps in the Giant Panda genome
Liu, P., Zhang, J., Cai, K., Wang, J., Liu, H., Zhang, L., Xu, W. F., Liu, Y., Shen, F., Hou, R., et al. (2026) · Communications Biology · doi:10.1038/s42003-026-09522-0
Fast bootstrap and reliable readout using hidden references for DNA data storage
Chen, W., Liu, S., Guo, Q., Qin, R., Ge, Q., Qi, T., & Yuan, Y. (2026) · iMeta · doi:10.1002/imt2.70105
Development and validation of high-density SNP array for genomic studies in Indian yak populations
Kumar, A., Dige, M., Arora, R., Niranjan, S., Ahlawat, S., Sharma, R., Kour, A., Ahmad, S. F., Raja, K., Singh, K. V., et al. (2026) · BMC Genomic Data · doi:10.1186/s12863-026-01404-y
“1) using BWA with default parameters [14].”
Metadata
- Authors
- Li, H., & Durbin, R.
- Affiliations
- Wellcome Sanger Institute (GB)
- Corresponding author
- Durbin, Richard
- Venue
- Bioinformatics
- Publisher
- Oxford University Press (OUP)
- Published
- 2010-01-15
- Volume
- 26
- Issue
- 5
- Pages
- 589-595
- ISSN
- 1367-4803 (ISSN-L)
- 1367-4811
- PMC
- PMC2828108
- OpenAlex
- W4247053599
- Cited by
- 12,063
- References
- 24
- Citations by year
- 2026: 639 · 2025: 972 · 2024: 1129 · 2023: 1067 · 2022: 1203 · 2021: 1245 · 2020: 1176 · 2019: 941 · 2018: 826 · 2017: 747 · 2016: 574 · 2015: 498 · 2014: 419 · 2013: 301 · 2012: 203
- FWCI
- 80.44
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Bioinformatics (publishedVersion, cc-by-nc)
- Funders
- Wellcome Trust (077192/Z/05/Z)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Physical Sciences › Mathematics › Theoretical Computer Science › Algorithms and Data Compression
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fractal and DNA sequence analysis
- Keywords
- long-read alignment, Burrows-Wheeler transform, Smith-Waterman alignment, sequence alignment, reference genome, blat, alignment speed, alignment accuracy, human genome
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