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Scott Schwartz
Scott Schwartz
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Bestätigte E-Mail-Adresse bei bx.psu.edu
Titel
Zitiert von
Zitiert von
Jahr
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
8514*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
61392000
Genome sequence of the Brown Norway rat yields insights into mammalian evolution
University of Utah Weiss Robert B. 14 Dunn Diane M. 14, ...
Nature 428 (6982), 493-521, 2004
25102004
Human–mouse alignments with BLASTZ
S Schwartz, WJ Kent, A Smit, Z Zhang, R Baertsch, RC Hardison, ...
Genome research 13 (1), 103-107, 2003
20022003
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
14052000
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), 983-987, 2018
10162018
Comparative analyses of multi-species sequences from targeted genomic regions
JW Thomas, JW Touchman, RW Blakesley, GG Bouffard, ...
Nature 424 (6950), 788-793, 2003
7872003
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
3572003
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
2752003
Why do miRNAs live in the miRNP?
DS Schwarz, PD Zamore
Genes & development 16 (9), 1025-1031, 2002
1842002
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
1742003
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
1631998
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
1042004
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
992002
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
992002
Comparison of human chromosome 21 conserved nongenic sequences (CNGs) with the mouse and dog genomes shows that their selective constraint is independent of their genic environment
ET Dermitzakis, E Kirkness, S Schwarz, E Birney, A Reymond, ...
Genome research 14 (5), 852-859, 2004
932004
Parallelization of a local similarity algorithm
X Huang, W Miller, S Schwartz, RC Hardison
Bioinformatics 8 (2), 155-165, 1992
901992
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
742001
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
PipTools: a computational toolkit to annotate and analyze pairwise comparisons of genomic sequences
L Elnitski, C Riemer, H Petrykowska, L Florea, S Schwartz, W Miller, ...
Genomics 80 (6), 681-690, 2002
562002
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