Scott Schwartz
Scott Schwartz
Unknown affiliation
Verified email at bx.psu.edu
TitleCited byYear
Initial sequencing and comparative analysis of the mouse genome
AT Chinwalla, LL Cook, KD Delehaunty, GA Fewell, LA Fulton, RS Fulton, ...
Nature 420 (6915), 520-562, 2002
6756*2002
Initial sequencing and comparative analysis of the mouse genome
AT Chinwalla, LL Cook, KD Delehaunty, GA Fewell, LA Fulton, RS Fulton, ...
Nature 420 (6915), 520-562, 2002
6756*2002
A greedy algorithm for aligning DNA sequences
Z Zhang, S Schwartz, L Wagner, W Miller
Journal of Computational biology 7 (1-2), 203-214, 2000
39552000
Genome sequence of the Brown Norway rat yields insights into mammalian evolution
Rat Genome Sequencing Project Consortium
Nature 428 (6982), 493, 2004
20552004
Human–mouse alignments with BLASTZ
S Schwartz, WJ Kent, A Smit, Z Zhang, R Baertsch, RC Hardison, ...
Genome research 13 (1), 103-107, 2003
13942003
PipMaker—a web server for aligning two genomic DNA sequences
S Schwartz, Z Zhang, KA Frazer, A Smit, C Riemer, J Bouck, R Gibbs, ...
Genome research 10 (4), 577-586, 2000
12822000
Comparative analyses of multi-species sequences from targeted genomic regions
JW Thomas, JW Touchman, RW Blakesley, GG Bouffard, ...
Nature 424 (6950), 788, 2003
7152003
Covariation in frequencies of substitution, deletion, transposition, and recombination during eutherian evolution
RC Hardison, KM Roskin, S Yang, M Diekhans, WJ Kent, R Weber, ...
Genome research 13 (1), 13-26, 2003
3202003
MultiPipMaker and supporting tools: Alignments and analysis of multiple genomic DNA sequences
S Schwartz, L Elnitski, M Li, M Weirauch, C Riemer, A Smit, NCS Program, ...
Nucleic acids research 31 (13), 3518-3524, 2003
2592003
Distinguishing regulatory DNA from neutral sites
L Elnitski, RC Hardison, J Li, S Yang, D Kolbe, P Eswara, MJ O'Connor, ...
Genome research 13 (1), 64-72, 2003
1692003
Comparative sequence analysis of a gene-rich cluster at human chromosome 12p13 and its syntenic region in mouse chromosome 6
MA Ansari-Lari, JC Oeltjen, S Schwartz, Z Zhang, DM Muzny, J Lu, ...
Genome Research 8 (1), 29-40, 1998
1511998
Generation and comparative analysis of∼ 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11. 23 implicated in Williams syndrome
U DeSilva, L Elnitski, JR Idol, JL Doyle, W Gan, JW Thomas, S Schwartz, ...
Genome research 12 (1), 3-15, 2002
912002
Generation and comparative analysis of∼ 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11. 23 implicated in Williams syndrome
U DeSilva, L Elnitski, JR Idol, JL Doyle, W Gan, JW Thomas, S Schwartz, ...
Genome research 12 (1), 3-15, 2002
912002
Patterns of insertions and their covariation with substitutions in the rat, mouse, and human genomes
S Yang, AF Smit, S Schwartz, F Chiaromonte, KM Roskin, D Haussler, ...
Genome research 14 (4), 517-527, 2004
812004
Parallelization of a local similarity algorithm
X Huang, W Miller, S Schwartz, RC Hardison
Bioinformatics 8 (2), 155-165, 1992
721992
A universal SNP and small-indel variant caller using deep neural networks
R Poplin, PC Chang, D Alexander, S Schwartz, T Colthurst, A Ku, ...
Nature biotechnology 36 (10), 983, 2018
682018
Comparative analysis of the gene-dense ACHE/TFR2 region on human chromosome 7q22 with the orthologous region on mouse chromosome 5
MD Wilson, C Riemer, DW Martindale, P Schnupf, AP Boright, TL Cheung, ...
Nucleic acids research 29 (6), 1352-1365, 2001
642001
GALA, a database for genomic sequence alignments and annotations
B Giardine, L Elnitski, C Riemer, I Makalowska, S Schwartz, W Miller, ...
Genome research 13 (4), 732-741, 2003
622003
Creating a universal SNP and small indel variant caller with deep neural networks
R Poplin, D Newburger, J Dijamco, N Nguyen, D Loy, SS Gross, ...
BioRxiv, 092890, 2016
542016
Analysis of conserved domains and sequence motifs in cellular regulatory proteins and locus control regions using new software tools for multiple alignment and visualization.
MS Boguski, RC Hardison, S Schwartz, W Miller
The New Biologist 4 (3), 247-260, 1992
521992
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Articles 1–20