1 sembled using a meta-assembly strategy after
sequencing of 10 lines derived from a maize-teosinte cro
2 We performed whole-genome
sequencing of 102 primary PanNETs and defined the genomi
3 Using whole-genome
sequencing of 11 262 Icelanders, we found 1403 cases of
4 Forty-six PMMs underwent targeted exome
sequencing of 111 cancer-associated genes.
5 enome variation map generated through genome
sequencing of 117 diverse accessions.
6 Transcriptome
sequencing of 120 cultivated and wild spinach accessions
7 Whole-exome and targeted
sequencing of 13 individuals from 10 unrelated families
8 RT-PCR
sequencing of 16 childhood ependymoma samples identified
9 Using single-molecule long-read
sequencing of 16 diverse fungal genomes, we observed tha
10 onhuman primates, we performed transcriptome
sequencing of 16 regions of adult human, chimpanzee, and
11 Marker gene
sequencing of 16S ribosomal genes revealed that the gut
12 . heliophila, using next-generation Illumina
sequencing of 16S rRNA gene sequences to characterize sy
13 High-throughput
sequencing of 16SrRNA genes demonstrated that plants in
14 de variants (SNVs) by conducting whole exome
sequencing of 18 trios consisting of Japanese patients w
15 oss of methicillin resistance through genome
sequencing of 180 isolates from 2016.
16 ecurrently mutated in 36 genes, and targeted
sequencing of 20 sites in 17,688 patients with NDD ident
17 lelic clusters, identified from whole-genome
sequencing of 228 DO mice.
18 Through comprehensive whole-transcriptome
sequencing of 231 children with acute lymphoblastic leuk
19 Here, we report the RNA
sequencing of 240 lettuce accessions sampled from the ma
20 Phylogenetic analysis based on whole-genome
sequencing of 250 isolates revealed two major M chimaera
21 this issue, we carried out 60x whole-genome
sequencing of 26 metastases from four patients with panc
22 new disease genes, we performed whole-exome
sequencing of 26 unrelated CG patients.
23 Targeted
sequencing of 283 genes was performed in 240 women with
24 Exome
sequencing of 291 parent-offspring trios with midline NS
25 Through deep
sequencing of 3' ends, we provide evidence that PARN can
26 erval) using high-depth (579x+/-315) nextgen
sequencing of 30 lung cancer and 89 control samples, res
27 We used molecular barcode
sequencing of 32 genes on the pretreatment peripheral bl
28 Whole-exome
sequencing of 33 unrelated patients with EoE revealed 39
29 Here, we report the targeted exome
sequencing of 330 genes, including genes known to be inv
30 an additional 182 families, and whole-genome
sequencing of 4 of the remaining 242 families revealed 2
31 Sequencing of 40 people with arhinia revealed that 84% o
32 2 SNPs derived from DNA resequencing and RNA-
sequencing of 41 groundnut accessions and wild diploid a
33 We performed whole-exome
sequencing of 43 unrelated probands affected by severe s
34 ng, targeted amplicon sequencing, and/or RNA-
sequencing of 46 pediatric primary MDS patients.
35 Exome
sequencing of 5 affected members identified a single nov
36 Here we report
sequencing of 5,205 samples from families with ASD, acco
37 re we perform whole-exome and -transcriptome
sequencing of 500 adult patients with metastatic solid t
38 Here we report targeted
sequencing of 59 DISC1 Interactome genes and 154 Regulom
39 Here we conducted a targeted exome-
sequencing of 63 trios of Chinese epilepsy families usin
40 on in 117 Wilms tumors, followed by targeted
sequencing of 651 Wilms tumors.
41 l dynamics using whole-exome and/or targeted
sequencing of 699 patients, of whom 122 were analyzed lo
42 tuary by rRNA and rDNA-based high throughput
sequencing of 97 samples collected along the entire sali
43 Whole exome and genome
sequencing of a 19-year-old girl (P7), initially diagnos
44 Whole-exome
sequencing of a breast cancer from a c.104T>C carrier re
45 on with selected advanced cancers, universal
sequencing of a broad panel of cancer-related genes in p
46 Sequencing of a cDNA encoding ArPPLNP2 revealed that it
47 ain-containing 2 (MAGI2) through whole-exome
sequencing of a deeply phenotyped cohort of patients wit
48 Sequencing of a distal IL1RL1 promoter region demonstrat
49 Through whole exome
sequencing of a family of three affected siblings with i
50 , Dudek et al. show that shotgun metagenomic
sequencing of a less-well-studied environment - dolphin
51 Here, we performed high-throughput RNA
sequencing of a Mabuya placenta transcriptome and screen
52 Sequencing of a P. malariae relative that infects chimpa
53 Here, we performed whole-exome
sequencing of a patient with disseminated Mycobacterium
54 Here, exome
sequencing of a single cohort of 2,871 CHD probands, inc
55 ring postnatal maturation by performing deep
sequencing of accessible chromatin regions by using the
56 r results show that timing and probabilistic
sequencing of actions can share the same neural circuits
57 Whole-genome
sequencing of all patients allowed exclusion of promiscu
58 We used RNA
sequencing of allelic six-rowed spike3 (vrs3) mutants wi
59 Here we describe the shotgun-
sequencing of ancient DNA from five specimens of Neander
60 ordances were clarified upon high-throughput
sequencing of antigen-receptor rearrangements and blind
61 Whole-genome bisulfite
sequencing of antigen-specific murine CD8 T cells at the
62 elative to the reference method (culture and
sequencing of any carbapenem-nonsusceptible isolate).
63 Sequencing of ARL15 in 375 severely insulin resistant pa
64 mporal cerebellar expression profiles by RNA
sequencing of ATXN2Q127 mice versus wild-type (WT) litte
65 As high-throughput
sequencing of B cells becomes more common, the need for
66 we focused on incorporating next-generation
sequencing of B-cell transcripts to determine the origin
67 High-throughput
sequencing of barcoded Kras (HDR) alleles from bulk lung
68 approach to this question by performing RNA
sequencing of brain tissue from mice chronically treated
69 been characterized across cancers by genome
sequencing of bulk tumors, including chronic lymphocytic
70 Moreover, RNA
sequencing of c-Kit(+) cells showed that CHD7 functions
71 The recent high-throughput
sequencing of cancer genomes and transcriptomes has prod
72 equencing (NGS) technology, such as targeted
sequencing of candidate cancer genes and whole-exome and
73 Single-cell
sequencing of cardiac CD45(-)c-kit(+) cells showed innat
74 RNA
sequencing of CD138(+) tumor cells from t(4;14)-positive
75 t of the transactivation domain of YAP1, and
sequencing of cDNA from the patient shows it does not re
76 Analysis of 16S ribosomal RNA gene
sequencing of cervicovaginal lavage clustered each parti
77 Whole genome
sequencing of CFW-passaged strains showed no specific ch
78 We used comparative whole-genome
sequencing of chemically mutagenized and natural Pgt iso
79 Finally,
sequencing of chromatin immunoprecipitates containing sp
80 those with advanced metastatic disease, deep
sequencing of circulating cell free DNA (cfDNA) obtained
81 Through massive shotgun
sequencing of circulating cell-free DNA from the blood,
82 ts with MM and healthy controls by small RNA
sequencing of circulating exosomes.
83 ing targeted clinical-grade, next-generation
sequencing of circulating tumor DNA (ctDNA).
84 at technological advances in next-generation
sequencing of circulating, tumor-derived nucleic acids h
85 laboratory conditions; and (4) whole-genome
sequencing of clinical and environmental isolates.
86 E, allowing proximity-dependent ligation and
sequencing of cognate sRNA-mRNA pairs as chimeric reads.
87 RNA
sequencing of cultured astrocytes derived from trkB.T1(+
88 l network, successful development involves a
sequencing of developmental events.
89 Small RNA
sequencing of dissected regions of immature seed coats d
90 ning systemic dsx knockdown, high-throughput
sequencing of diverse tissues and a genome-wide analysis
91 Short- and long-read high-throughput
sequencing of DNA and RNA demonstrated that the chloropl
92 Here, we show whole-genome
sequencing of DNA and RNA in 94 Chinese individuals with
93 Methods for next-generation
sequencing of DNA are producing a wealth of information
94 Metagenomics, the
sequencing of DNA extracted directly from natural microb
95 Multiplexed tag-encoded
sequencing of DNA from the samples was performed, and th
96 chromosome pairs allows for the independent
sequencing of each of the complementary and homologous s
97 Sequencing of ELF3 in ICCV 96029 revealed an 11-bp delet
98 m(6)A
sequencing of embryonic mouse cortex reveals enrichment
99 demonstration of tandem ME-SIMS for de novo
sequencing of endogenous neuropeptides from tissue in si
100 This method combines de novo MS/MS
sequencing of enriched antibodies and co-extracted prote
101 High-throughput amplicon
sequencing of environmental DNA (eDNA metabarcoding) rep
102 Large-scale
sequencing of environmental microbiomes has the potentia
103 Single-cell RNA
sequencing of epidermal progenitors revealed the emergen
104 RNA
sequencing of Erdr1-overexpressing cells identified the
105 Bisulfite
sequencing of exposed and control animals highlighted di
106 We are performing whole-genome
sequencing of families with autism spectrum disorder (AS
107 de novo mutations discovered by large-scale
sequencing of family samples, 215 genes spanning rare an
108 V4 16S rRNA gene
sequencing of fecal DNA demonstrated minimal shifts in t
109 Sequencing of fern mitogenomes could shed light on the m
110 cteristics were observed for next-generation
sequencing of FFPET, whole blood, and dried blood spot i
111 Sequencing of FGFR1 identified a previously unreported d
112 ed NO and N2 O to varying degrees and genome
sequencing of four indicated that two isolates held gene
113 ed and analyzed, enables fast and affordable
sequencing of full human genomes.
114 Further, small RNA
sequencing of GBM patients identified significant miRNA
115 Targeted exome
sequencing of genes encoding the mitochondrial proteome
116 Precision Oncology relies on indiscriminate
sequencing of genomes in biopsies that barely represent
117 Sequencing of genomic DNA from the infant's saliva yield
118 We demonstrate ultra-high-throughput
sequencing of &
gt;50,000 cells per run in a synthetic commu
119 Metagenomic next generation
sequencing of his cerebrospinal fluid and brain biopsy t
120 Deep
sequencing of HIV reverse transcriptase (RT) was perform
121 Whole exome
sequencing of HLHS fibroblasts identified deleterious va
122 this methodology particularly useful for the
sequencing of HS saccharides, because the lack of contam
123 We perform single-cell RNA-
sequencing of human gliomas and identify phenotypic diff
124 ecovered using UV-crosslinking, ligation and
sequencing of hybrids (CLASH).
125 althy controls, we performed high-throughput
sequencing of immunoglobulin heavy chain VDJ rearrangeme
126 Large-scale DNA
sequencing of immunological repertoires offers an opport
127 Metagenomic
sequencing of incubation samples revealed that LREE-cont
128 Sequencing of independent clonal isolates of replication
129 Autozygosity mapping in families and exome
sequencing of index patients were performed in 152 consa
130 Dual RNA
sequencing of individual host cell populations and C. al
131 Moreover, exome
sequencing of individuals with idiopathic SZ identified
132 By next-generation
sequencing of infected tissue homogenates, we assembled
133 formally identified by PCR amplification and
sequencing of internal transcribed spacer 1 (ITS1), was
134 -type mice and performed high throughput RNA-
Sequencing of kidney tissue in aged mice.
135 Next generation
sequencing of Kupffer cell miRNA identified miRNA 181b-3
136 Targeted
sequencing of LAMB4 in 148 non-familial and unrelated sp
137 Sequencing of LanFTc1 revealed a 1.4-kb deletion in the
138 primers enable massively parallel, targeted
sequencing of large STR sets.
139 c leukemia (T-ALL), but detailed genome-wide
sequencing of large T-ALL cohorts has not been carried o
140 vertebrate species, we used single-cell RNA
sequencing of lck:GFP cells in zebrafish and obtained th
141 In conclusion, 454-deep
sequencing of liver and plasma compartments in treatment
142 Similarly, RNA
sequencing of lupus patient blood revealed similar expre
143 We performed RNA
sequencing of lupus patient whole blood to determine com
144 Deep
sequencing of lymphocyte receptor repertoires has made i
145 An important feature in
sequencing of mAbs is the discrimination of isobaric res
146 Here we use highly parallel, single-cell RNA
sequencing of malaria cultures undergoing sexual commitm
147 combination of community fingerprinting and
sequencing of marker genes to identify community changes
148 Here, we analyze whole exome
sequencing of matched pre- and post-neoadjuvant cisplati
149 nt and convenient method for high-throughput
sequencing of mature tRNAs.
150 tro microbiology approaches and whole-genome
sequencing of Methanomicrobium mobile, a key species wit
151 Sequencing of methylomes, transcriptomes, and genomes of
152 study of the human microbiome through direct
sequencing of microbial DNA, resulting in an enormous am
153 High-throughput DNA
sequencing of microbiota from a diverse collection of fe
154 Here we used Next Generation
Sequencing of microRNAs to identify negative regulators
155 miR-seq (deep
sequencing of miRNAs) data reveal that the degradation o
156 Isolation and next-generation
sequencing of MIWI2-positive multiciliated cells reveale
157 Here, Patel et al. use targeted DNA
sequencing of MODY patients and large-scale publically a
158 A high-throughput
sequencing of mRNAs was performed to investigate the eff
159 Here, we employed genomic DNA
sequencing of multiple variable (V) regions of the bacte
160 ely 10,000 cells) whole-genome shotgun (WGS)
sequencing of Mycobacterium tuberculosis and soil micro-
161 Deep
sequencing of nasopharyngeal samples produced partial se
162 Here we conduct exome
sequencing of nine non-serous epithelial ovarian tumors
163 RNA
sequencing of NOD.Abd3 common bile duct early in disease
164 We further performed whole-genome
sequencing of nosocomial MDRPa strains to evaluate genot
165 Population-based sequencing and 454 deep
sequencing of NS5B gene were performed on plasma and liv
166 ed for comparative chromatin biology because
sequencing of numerous genomes from many clades is coupl
167 Sequencing of OG paves the way to address chemical and b
168 Sequencing of one molecular type (RNA, methylated DNA or
169 herefore ideal for fast and massive parallel
sequencing of parasite transcriptomes directly from host
170 se mutations can be best identified by exome
sequencing of parent-offspring trios.
171 Targeted deep
sequencing of parental fibroblasts revealed that most va
172 characterized by next-generation (Illumina)
sequencing of partial (V4) 16S rRNA gene sequences.
173 Fast, affordable
sequencing of pathogen genomes - now a staple of the pub
174 study highlights the power of data from deep
sequencing of pathogens as a component of outbreak inves
175 Whole-genome
sequencing of pathogens from host samples becomes more a
176 tation of the human genome and transition to
sequencing of patient genomes instead of exomes will be
177 Using information from deep
sequencing of patients with neurological or psychiatric
178 In this study, the
sequencing of PCR amplicons generated using primers targ
179 Conventional Sanger
sequencing of PCR products is the gold standard for spec
180 the performance of pY-MIP for enrichment and
sequencing of phosphopeptides obtained by tryptic digest
181 Using RNA-
sequencing of platelets followed by validation via RT-PC
182 enomes of single cells, followed by Illumina
sequencing of pooled DNA.
183 We conclude that DNA
sequencing of pooled samples of large numbers of bacteri
184 Using RNA
sequencing of Populus trichocarpa roots in mutualistic s
185 However, exome
sequencing of PP;Trp53 KO melanomas failed to reveal any
186 ripotent cells in vivo, obtained by the deep
sequencing of pre-implantation embryos.
187 Ultra-deep targeted next generation
sequencing of pretreatment plasma cfDNA from DLBCL patie
188 Plasmid DNA
sequencing of previously uncharacterized clinical extend
189 Whole-genome bisulfite
sequencing of primary human naive, short-lived effector
190 genesis, we performed whole-genome bisulfite
sequencing of primary leukemic and non-leukemic cells in
191 o-HCT was profiled by means of 16S ribosomal
sequencing of prospectively collected stool samples.
192 to oligosaccharide standards and to de novo
sequencing of purified plant metabolite glycoconjugates,
193 RNA
sequencing of resident CD45(-) joint cells from advanced
194 Ultra-deep
sequencing of resistant parasites identifies the sarco/e
195 analysis, an unbiased approach based on RNA
sequencing of resistant subclones, to discover the molec
196 ration chromatin immunoprecipitation and RNA
sequencing of reward brain regions indicates that the re
197 Using RNA
sequencing of ribosome-bound mRNA from hippocampal CA3 n
198 se and can be measured using next-generation
sequencing of RNA (RNA-seq).
199 Using high-throughput
sequencing of RNA isolated by crosslinking immunoprecipi
200 High-throughput
sequencing of RNA prepared using RPAD from human cervica
201 ions were identified through next-generation
sequencing of saliva or blood samples, and RNA was extra
202 In conclusion, whole-genome
sequencing of samples obtained following neoadjuvant che
203 tivity of HALE estimates was assessed to the
sequencing of select comorbidities for the dependent com
204 P calls closely concordant with whole-genome
sequencing of selected lines.
205 Amplicon
sequencing of selected samples revealed the prevalence o
206 Amplicon
sequencing of several independent saddle pattern mutants
207 We used high-throughput
sequencing of short, cyclobutane pyrimidine dimer-contai
208 encing technologies such as exome and genome
sequencing of similar patient cohorts will reveal additi
209 n this study, we demonstrate that sparse DNA
sequencing of single-cell nuclei from prostate core biop
210 Deep
sequencing of size-selected DNase I-treated chromatin (D
211 In the present study, we performed deep
sequencing of small RNA molecules in the embryonic fibro
212 Here, using high-throughput marker gene
sequencing of soils collected from 18 sites throughout N
213 l abnormalities that suggest a syndrome, and
sequencing of specific genes or next-generation sequenci
214 Deep
sequencing of Spo11 oligonucleotides demonstrates that T
215 ion of these compounds based on whole genome
sequencing of spontaneous resistant mutants, which ident
216 nd spp3 revealed they were allelic, and deep
sequencing of spp3 identified an independent disruptive
217 Finally, RNA
sequencing of ST18-depleted tumors before involution rev
218 were determined using metatranscriptomic RNA
sequencing of stomach biopsy specimens from individuals
219 rmed gene expression profile analysis by RNA
sequencing of subsets of interferon gamma (IFNG)-produci
220 ssessed by both 16S rDNA and metagenomic DNA
sequencing, of TB cases during antimycobacterial treatme
221 High-throughput
sequencing of TEM-1 populations shows that this advantag
222 Exome
sequencing of Tet2(-/-) tumours reveals accumulation of
223 Each participant underwent targeted
sequencing of TGM1.
224 ion of flow cytometric cell sorting and deep
sequencing of the 16S rDNA gene was used to characterize
225 y, bacterial composition was identified with
sequencing of the 16S ribosomal RNA gene in breast milk,
226 east milk, areolar skin, and infant stool by
sequencing of the 16S ribosomal RNA gene.
227 Using next-generation DNA
sequencing of the 16S rRNA gene, we analyzed the composi
228 Sequencing of the 16S-rRNA components of this aerosol re
229 Sequencing of the 3'UTR of common HLA-A alleles indicate
230 Sanger
sequencing of the AH cfDNA and tumor DNA with polymerase
231 e isolated and characterized using RAPDs and
sequencing of the almost complete 16S rRNA gene.
232 DNA
sequencing of the APOC2 gene in the patient and one of h
233 tes in combination with improvements in deep
sequencing of the autologous cancer have provided new in
234 RNA
sequencing of the basolateral amygdala revealed transcri
235 ctivation by Fos immunofluorescence, and RNA
sequencing of the basolateral amygdala.
236 opose that the information generated by deep
sequencing of the BBCE cell lines coupled with phenotypi
237 To address this question, we performed deep
sequencing of the BCR repertoire of AChR-MG, MuSK-MG, an
238 We performed high-throughput deep
sequencing of the beta-TCR repertoire in 29 lesional and
239 cross-linked to RNA in vivo High-throughput
sequencing of the bound RNAs revealed strong Set1 enrich
240 quencing in an IO IBD patient and subsequent
sequencing of the candidate gene in 12 additional IO IBD
241 Sequencing of the coding regions of all linked genes fai
242 Nevertheless, during our isolation and
sequencing of the complete genome of faustovirus, follow
243 Sequencing of the deletions caused by CRISPR-Cas self ta
244 ficance, informational content, and temporal
sequencing of the different types of movement in dance.
245 evidence for trait association from complete
sequencing of the DISC1 locus.
246 Sequencing of the dynemicin biosynthetic gene cluster in
247 Recent
sequencing of the fiber-degrading Ruminococcus flavefaci
248 Using amplicon
sequencing of the fungal internal transcribed spacer 2,
249 Sequencing of the HAstV-2 capsid genes reveals mutations
250 More than a decade after the
sequencing of the human genome, a deluge of genome-wide
251 Quantitative deep
sequencing of the Ig heavy chain locus from B220(+)CD43(
252 Genome
sequencing of the immigrant identified it as a G. coniro
253 Sanger
sequencing of the LAT gene showed a mutation that result
254 To study this, we performed next generation
sequencing of the livers of Sprague-Dawley rats treated
255 DNA
sequencing of the lysozyme gene in the patient and his m
256 ne strains, and field isolates, whole-genome
sequencing of the M. gallisepticum vaccine strain ts-11
257 oreover, whole exome sequencing and targeted
sequencing of the major pancreatic cysts has identified
258 ChIP
sequencing of the major players NUT, ZNF532, BRD4, EP300
259 make it possible to analyse high-throughput
sequencing of the methylome of any given organism under
260 We performed DNA
sequencing of the ORAI1 gene, modeling of mutations on O
261 We believe we report the first transcriptome
sequencing of the postmortem human dorsal striatum compa
262 Here we used whole-genome
sequencing of the proposed serovar 16 reference strain A
263 Direct
sequencing of the purified DNA segments can have >100-fo
264 Sequencing of the recovered ssODNs provided quantitative
265 Whole-exome
sequencing of the remaining 424 families revealed mutati
266 We report the
sequencing of the Stentor coeruleus macronuclear genome
267 Sequencing of the switch regions of memory B cells from
268 Sequencing of the syncytial variants revealed mutations
269 herited variants detected using simultaneous
sequencing of the tumor and normal tissue ("tumor-normal
270 Deep
sequencing of the tumor genome showed a highly heterogen
271 to compare bacterial load and Illumina MiSeq
sequencing of the V1-V3 regions of the 16S rRNA gene use
272 s were collected and analyzed using 16S rRNA
sequencing of the V3-V4 hypervariable region.
273 MiSeq
sequencing of the V4 region of both bacterial and archae
274 mposition was assessed via amplification and
sequencing of the V4 region of the 16S ribosomal RNA gen
275 Sanger-based
sequencing of the viral protein 1 (VP1) capsid region is
276 Pyrosequencing genotyping and
sequencing of the voltage gated sodium channel (VGSC) ge
277 Sanger
sequencing of this candidate gene in independent allelic
278 Whole-genome
sequencing of three mangrove species further shows the d
279 We perform RNA
sequencing of tissues from American alligator embryos to
280 We assessed if metagenomic
sequencing of total DNA extracts obtained direct from so
281 tive and quantitative method for single-cell
sequencing of total RNA.
282 RNA
sequencing of TPB-resistant tumors revealed that extrace
283 additives to feedlot cattle using metagenome
sequencing of treated and control animals.
284 Next-generation
sequencing of tumors and matched normal DNA.
285 Next-generation
sequencing of tumors as part of clinical care included h
286 ways that would not be as apparent from bulk
sequencing of tumors, and can potentially establish whet
287 cted genome-wide mRNA profiling and DNA exon
sequencing of two cell lines (TMD and BMD) derived from
288 We also report the
sequencing of two diploids from the ancestral gene pools
289 Exome
sequencing of two Finnish sisters with non-syndromic POI
290 Ultra-deep
sequencing of two healthy-looking skin biopsies identifi
291 a major mitochondrial DNA (mtDNA) survey and
sequencing of two nuclear markers (AME and RAG-1) from P
292 is remarkable property is applied to de novo
sequencing of underivatized oligosaccharides.Establishin
293 Whole genome
sequencing of UNG/SMUG1-deficient tumours revealed that
294 anscriptional dynamics using single-cell RNA
sequencing of unstimulated and stimulated naive and effe
295 nature, we performed whole-transcriptome RNA
sequencing of untreated, apoptotic, and recovering HeLa
296 Sequencing of viral nucleic acids from the stool of vacc
297 ore relatively recently, coinciding with the
sequencing of whole genomes.
298 vercomes this drawback by untargeted shotgun
sequencing of whole metagenomes at affordable cost.
299 ve structural diversity arises, we used deep
sequencing of wild populations to reveal genetic variati
300 lecular basis for abnormal KSC function, RNA
sequencing of wild-type (WT) and VDR(-/-) KSCs was perfo